Name: rs760293
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs760293

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:31644000 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: T>A / T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.195414 (51724/264690, TOPMED)
T=0.161936 (40442/249740, GnomAD_exome)
T=0.167354 (38414/229538, ALFA) (+ 22 more)
T=0.194872 (27291/140046, GnomAD)
T=0.163838 (19657/119978, ExAC)
T=0.19445 (15303/78698, PAGE_STUDY)
T=0.07623 (2154/28258, 14KJPN)
T=0.07542 (1264/16760, 8.3KJPN)
T=0.2033 (1716/8440, GO-ESP)
T=0.1827 (1170/6404, 1000G_30x)
T=0.1787 (895/5008, 1000G)
T=0.1699 (761/4480, Estonian)
T=0.1751 (675/3854, ALSPAC)
T=0.1726 (640/3708, TWINSUK)
T=0.1099 (322/2930, KOREAN)
T=0.172 (172/998, GoNL)
T=0.148 (117/790, PRJEB37584)
T=0.183 (110/600, NorthernSweden)
T=0.114 (61/536, SGDP_PRJ)
T=0.137 (73/534, MGP)
T=0.361 (78/216, Qatari)
T=0.300 (63/210, Vietnamese)
T=0.03 (2/72, Ancient Sardinia)
T=0.17 (9/54, Siberian)
T=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BAG6 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	229632	T=0.167320	C=0.832680
European	Sub	193416	T=0.166062	C=0.833938
African	Sub	5960	T=0.2698	C=0.7302
African Others	Sub	206	T=0.325	C=0.675
African American	Sub	5754	T=0.2678	C=0.7322
Asian	Sub	6682	T=0.1521	C=0.8479
East Asian	Sub	4798	T=0.1403	C=0.8597
Other Asian	Sub	1884	T=0.1821	C=0.8179
Latin American 1	Sub	714	T=0.167	C=0.833
Latin American 2	Sub	7410	T=0.1374	C=0.8626
South Asian	Sub	336	T=0.161	C=0.839
Other	Sub	15114	T=0.16462	C=0.83538

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.195414	C=0.804586
gnomAD - Exomes	Global	Study-wide	249740	T=0.161936	C=0.838064
gnomAD - Exomes	European	Sub	134150	T=0.161223	C=0.838777
gnomAD - Exomes	Asian	Sub	48942	T=0.16812	C=0.83188
gnomAD - Exomes	American	Sub	34500	T=0.12583	C=0.87417
gnomAD - Exomes	African	Sub	16016	T=0.27192	C=0.72808
gnomAD - Exomes	Ashkenazi Jewish	Sub	10036	T=0.09067	C=0.90933
gnomAD - Exomes	Other	Sub	6096	T=0.1608	C=0.8392
Allele Frequency Aggregator	Total	Global	229538	T=0.167354	C=0.832646
Allele Frequency Aggregator	European	Sub	193340	T=0.166086	C=0.833914
Allele Frequency Aggregator	Other	Sub	15096	T=0.16481	C=0.83519
Allele Frequency Aggregator	Latin American 2	Sub	7410	T=0.1374	C=0.8626
Allele Frequency Aggregator	Asian	Sub	6682	T=0.1521	C=0.8479
Allele Frequency Aggregator	African	Sub	5960	T=0.2698	C=0.7302
Allele Frequency Aggregator	Latin American 1	Sub	714	T=0.167	C=0.833
Allele Frequency Aggregator	South Asian	Sub	336	T=0.161	C=0.839
gnomAD - Genomes	Global	Study-wide	140046	T=0.194872	C=0.805128
gnomAD - Genomes	European	Sub	75882	T=0.16593	C=0.83407
gnomAD - Genomes	African	Sub	41916	T=0.27173	C=0.72827
gnomAD - Genomes	American	Sub	13644	T=0.15501	C=0.84499
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.0981	C=0.9019
gnomAD - Genomes	East Asian	Sub	3128	T=0.1509	C=0.8491
gnomAD - Genomes	Other	Sub	2152	T=0.1845	C=0.8155
ExAC	Global	Study-wide	119978	T=0.163838	C=0.836162
ExAC	Europe	Sub	72384	T=0.15629	C=0.84371
ExAC	Asian	Sub	25078	T=0.16596	C=0.83404
ExAC	American	Sub	11520	T=0.11849	C=0.88151
ExAC	African	Sub	10102	T=0.26638	C=0.73362
ExAC	Other	Sub	894	T=0.141	C=0.859
The PAGE Study	Global	Study-wide	78698	T=0.19445	C=0.80555
The PAGE Study	AfricanAmerican	Sub	32516	T=0.26747	C=0.73253
The PAGE Study	Mexican	Sub	10810	T=0.12840	C=0.87160
The PAGE Study	Asian	Sub	8318	T=0.0981	C=0.9019
The PAGE Study	PuertoRican	Sub	7918	T=0.1692	C=0.8308
The PAGE Study	NativeHawaiian	Sub	4534	T=0.0946	C=0.9054
The PAGE Study	Cuban	Sub	4228	T=0.1786	C=0.8214
The PAGE Study	Dominican	Sub	3828	T=0.2254	C=0.7746
The PAGE Study	CentralAmerican	Sub	2448	T=0.1544	C=0.8456
The PAGE Study	SouthAmerican	Sub	1982	T=0.1387	C=0.8613
The PAGE Study	NativeAmerican	Sub	1260	T=0.1722	C=0.8278
The PAGE Study	SouthAsian	Sub	856	T=0.169	C=0.831
14KJPN	JAPANESE	Study-wide	28258	T=0.07623	C=0.92377
8.3KJPN	JAPANESE	Study-wide	16760	T=0.07542	C=0.92458
GO Exome Sequencing Project	Global	Study-wide	8440	T=0.2033	C=0.7967
GO Exome Sequencing Project	European American	Sub	5418	T=0.1715	C=0.8285
GO Exome Sequencing Project	African American	Sub	3022	T=0.2604	C=0.7396
1000Genomes_30x	Global	Study-wide	6404	T=0.1827	C=0.8173
1000Genomes_30x	African	Sub	1786	T=0.2800	C=0.7200
1000Genomes_30x	Europe	Sub	1266	T=0.1564	C=0.8436
1000Genomes_30x	South Asian	Sub	1202	T=0.1339	C=0.8661
1000Genomes_30x	East Asian	Sub	1170	T=0.1556	C=0.8444
1000Genomes_30x	American	Sub	980	T=0.132	C=0.868
1000Genomes	Global	Study-wide	5008	T=0.1787	C=0.8213
1000Genomes	African	Sub	1322	T=0.2738	C=0.7262
1000Genomes	East Asian	Sub	1008	T=0.1607	C=0.8393
1000Genomes	Europe	Sub	1006	T=0.1501	C=0.8499
1000Genomes	South Asian	Sub	978	T=0.132	C=0.868
1000Genomes	American	Sub	694	T=0.131	C=0.869
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.1699	C=0.8301
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.1751	C=0.8249
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.1726	C=0.8274
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.1099	A=0.0000, C=0.8901, G=0.0000
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.172	C=0.828
CNV burdens in cranial meningiomas	Global	Study-wide	790	T=0.148	C=0.852
CNV burdens in cranial meningiomas	CRM	Sub	790	T=0.148	C=0.852
Northern Sweden	ACPOP	Study-wide	600	T=0.183	C=0.817
SGDP_PRJ	Global	Study-wide	536	T=0.114	C=0.886
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.137	C=0.863
Qatari	Global	Study-wide	216	T=0.361	C=0.639
A Vietnamese Genetic Variation Database	Global	Study-wide	210	T=0.300	C=0.700
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	72	T=0.03	C=0.97
Siberian	Global	Study-wide	54	T=0.17	C=0.83
The Danish reference pan genome	Danish	Study-wide	40	T=0.20	C=0.80

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 6	NC_000006.12:g.31644000T>A
GRCh38.p14 chr 6	NC_000006.12:g.31644000T>C
GRCh38.p14 chr 6	NC_000006.12:g.31644000T>G
GRCh37.p13 chr 6	NC_000006.11:g.31611777T>A
GRCh37.p13 chr 6	NC_000006.11:g.31611777T>C
GRCh37.p13 chr 6	NC_000006.11:g.31611777T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.3121289C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.3121289C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.3121289C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.3121395C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.3121395C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.3121395C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2899821C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2899821C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2899821C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2905417C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2905417C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2905417C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.2:g.2891766C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.2:g.2891766C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.2:g.2891766C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.1:g.2897351C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.1:g.2897351C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.1:g.2897351C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.2943284C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.2943284C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.2943284C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.2942582C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.2942582C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.2942582C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2949046C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2949046C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2949046C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2954666C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2954666C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2954666C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.2985865C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.2985865C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.2985865C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.2991450C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.2991450C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.2991450C>G

Gene: BAG6, BAG cochaperone 6 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BAG6 transcript variant 4	NM_001098534.2:c.1561-23A… NM_001098534.2:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 5	NM_001199697.2:c.1561-26A… NM_001199697.2:c.1561-26A>T	N/A	Intron Variant
BAG6 transcript variant 6	NM_001199698.2:c.1561-23A… NM_001199698.2:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 7	NM_001387940.1:c.1561-23A… NM_001387940.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 8	NM_001387942.1:c.1507-26A… NM_001387942.1:c.1507-26A>T	N/A	Intron Variant
BAG6 transcript variant 9	NM_001387943.1:c.1669-23A… NM_001387943.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 10	NM_001387944.1:c.1507-23A… NM_001387944.1:c.1507-23A>T	N/A	Intron Variant
BAG6 transcript variant 11	NM_001387946.1:c.1669-23A… NM_001387946.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 12	NM_001387949.1:c.1561-26A… NM_001387949.1:c.1561-26A>T	N/A	Intron Variant
BAG6 transcript variant 13	NM_001387951.1:c.1561-23A… NM_001387951.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 14	NM_001387954.1:c.1669-23A… NM_001387954.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 15	NM_001387955.1:c.1561-26A… NM_001387955.1:c.1561-26A>T	N/A	Intron Variant
BAG6 transcript variant 16	NM_001387956.1:c.1561-23A… NM_001387956.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 17	NM_001387958.1:c.1615-23A… NM_001387958.1:c.1615-23A>T	N/A	Intron Variant
BAG6 transcript variant 18	NM_001387961.1:c.1561-23A… NM_001387961.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 19	NM_001387963.1:c.1507-26A… NM_001387963.1:c.1507-26A>T	N/A	Intron Variant
BAG6 transcript variant 20	NM_001387964.1:c.1507-23A… NM_001387964.1:c.1507-23A>T	N/A	Intron Variant
BAG6 transcript variant 21	NM_001387965.1:c.1669-23A… NM_001387965.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 22	NM_001387982.1:c.1507-23A… NM_001387982.1:c.1507-23A>T	N/A	Intron Variant
BAG6 transcript variant 23	NM_001387983.1:c.1669-26A… NM_001387983.1:c.1669-26A>T	N/A	Intron Variant
BAG6 transcript variant 24	NM_001387984.1:c.1669-23A… NM_001387984.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 25	NM_001387985.1:c.1696-23A… NM_001387985.1:c.1696-23A>T	N/A	Intron Variant
BAG6 transcript variant 26	NM_001387986.1:c.1561-23A… NM_001387986.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 27	NM_001387987.1:c.1561-26A… NM_001387987.1:c.1561-26A>T	N/A	Intron Variant
BAG6 transcript variant 28	NM_001387988.1:c.1669-26A… NM_001387988.1:c.1669-26A>T	N/A	Intron Variant
BAG6 transcript variant 29	NM_001387989.1:c.1669-23A… NM_001387989.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 30	NM_001387990.1:c.1561-26A… NM_001387990.1:c.1561-26A>T	N/A	Intron Variant
BAG6 transcript variant 31	NM_001387991.1:c.1615-23A… NM_001387991.1:c.1615-23A>T	N/A	Intron Variant
BAG6 transcript variant 32	NM_001387992.1:c.1615-23A… NM_001387992.1:c.1615-23A>T	N/A	Intron Variant
BAG6 transcript variant 33	NM_001387993.1:c.1669-26A… NM_001387993.1:c.1669-26A>T	N/A	Intron Variant
BAG6 transcript variant 34	NM_001387994.1:c.1669-23A… NM_001387994.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 35	NM_001387995.1:c.1669-26A… NM_001387995.1:c.1669-26A>T	N/A	Intron Variant
BAG6 transcript variant 36	NM_001387996.1:c.1669-23A… NM_001387996.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 37	NM_001387997.1:c.1507-23A… NM_001387997.1:c.1507-23A>T	N/A	Intron Variant
BAG6 transcript variant 38	NM_001387998.1:c.1561-26A… NM_001387998.1:c.1561-26A>T	N/A	Intron Variant
BAG6 transcript variant 39	NM_001387999.1:c.1561-23A… NM_001387999.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 40	NM_001388000.1:c.1561-26A… NM_001388000.1:c.1561-26A>T	N/A	Intron Variant
BAG6 transcript variant 41	NM_001388001.1:c.1561-23A… NM_001388001.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 42	NM_001388002.1:c.1483-26A… NM_001388002.1:c.1483-26A>T	N/A	Intron Variant
BAG6 transcript variant 43	NM_001388003.1:c.1483-23A… NM_001388003.1:c.1483-23A>T	N/A	Intron Variant
BAG6 transcript variant 44	NM_001388004.1:c.1507-23A… NM_001388004.1:c.1507-23A>T	N/A	Intron Variant
BAG6 transcript variant 45	NM_001388005.1:c.1669-26A… NM_001388005.1:c.1669-26A>T	N/A	Intron Variant
BAG6 transcript variant 46	NM_001388006.1:c.1669-23A… NM_001388006.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 47	NM_001388007.1:c.1561-26A… NM_001388007.1:c.1561-26A>T	N/A	Intron Variant
BAG6 transcript variant 48	NM_001388008.1:c.1588-26A… NM_001388008.1:c.1588-26A>T	N/A	Intron Variant
BAG6 transcript variant 49	NM_001388009.1:c.1588-23A… NM_001388009.1:c.1588-23A>T	N/A	Intron Variant
BAG6 transcript variant 50	NM_001388010.1:c.1669-26A… NM_001388010.1:c.1669-26A>T	N/A	Intron Variant
BAG6 transcript variant 51	NM_001388011.1:c.1669-23A… NM_001388011.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 52	NM_001388012.1:c.1696-23A… NM_001388012.1:c.1696-23A>T	N/A	Intron Variant
BAG6 transcript variant 53	NM_001388013.1:c.1507-26A… NM_001388013.1:c.1507-26A>T	N/A	Intron Variant
BAG6 transcript variant 54	NM_001388014.1:c.1561-23A… NM_001388014.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 55	NM_001388015.1:c.1561-23A… NM_001388015.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 56	NM_001388016.1:c.1669-26A… NM_001388016.1:c.1669-26A>T	N/A	Intron Variant
BAG6 transcript variant 57	NM_001388017.1:c.1561-23A… NM_001388017.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 58	NM_001388018.1:c.1561-23A… NM_001388018.1:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 59	NM_001388019.1:c.1669-26A… NM_001388019.1:c.1669-26A>T	N/A	Intron Variant
BAG6 transcript variant 60	NM_001388020.1:c.1669-23A… NM_001388020.1:c.1669-23A>T	N/A	Intron Variant
BAG6 transcript variant 2	NM_080702.3:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant 3	NM_080703.3:c.1561-23A>T	N/A	Intron Variant
BAG6 transcript variant X12	XM_017011296.2:c.1561-26A… XM_017011296.2:c.1561-26A>T	N/A	Intron Variant
BAG6 transcript variant X9	XM_017011297.2:c.1615-26A… XM_017011297.2:c.1615-26A>T	N/A	Intron Variant
BAG6 transcript variant X1	XM_047419338.1:c.1615-23A… XM_047419338.1:c.1615-23A>T	N/A	Intron Variant
BAG6 transcript variant X2	XM_047419339.1:c.1615-26A… XM_047419339.1:c.1615-26A>T	N/A	Intron Variant
BAG6 transcript variant X3	XM_047419340.1:c.1615-26A… XM_047419340.1:c.1615-26A>T	N/A	Intron Variant
BAG6 transcript variant X4	XM_047419341.1:c.1669-26A… XM_047419341.1:c.1669-26A>T	N/A	Intron Variant
BAG6 transcript variant X5	XM_047419342.1:c.1507-26A… XM_047419342.1:c.1507-26A>T	N/A	Intron Variant
BAG6 transcript variant X6	XM_047419343.1:c.1507-26A… XM_047419343.1:c.1507-26A>T	N/A	Intron Variant
BAG6 transcript variant X7	XM_047419344.1:c.1615-23A… XM_047419344.1:c.1615-23A>T	N/A	Intron Variant
BAG6 transcript variant X8	XM_047419345.1:c.1615-23A… XM_047419345.1:c.1615-23A>T	N/A	Intron Variant
BAG6 transcript variant X10	XM_047419346.1:c.1615-26A… XM_047419346.1:c.1615-26A>T	N/A	Intron Variant
BAG6 transcript variant X11	XM_047419347.1:c.1615-26A… XM_047419347.1:c.1615-26A>T	N/A	Intron Variant
BAG6 transcript variant X13	XM_047419348.1:c.1507-23A… XM_047419348.1:c.1507-23A>T	N/A	Intron Variant
BAG6 transcript variant X14	XM_047419349.1:c.1507-26A… XM_047419349.1:c.1507-26A>T	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	T=	A	C	G
GRCh38.p14 chr 6	NC_000006.12:g.31644000=	NC_000006.12:g.31644000T>A	NC_000006.12:g.31644000T>C	NC_000006.12:g.31644000T>G
GRCh37.p13 chr 6	NC_000006.11:g.31611777=	NC_000006.11:g.31611777T>A	NC_000006.11:g.31611777T>C	NC_000006.11:g.31611777T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.3121289C>T	NT_113891.3:g.3121289C>A	NT_113891.3:g.3121289=	NT_113891.3:g.3121289C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.3121395C>T	NT_113891.2:g.3121395C>A	NT_113891.2:g.3121395=	NT_113891.2:g.3121395C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2899821C>T	NT_167248.2:g.2899821C>A	NT_167248.2:g.2899821=	NT_167248.2:g.2899821C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2905417C>T	NT_167248.1:g.2905417C>A	NT_167248.1:g.2905417=	NT_167248.1:g.2905417C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.2:g.2891766C>T	NT_167245.2:g.2891766C>A	NT_167245.2:g.2891766=	NT_167245.2:g.2891766C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.1:g.2897351C>T	NT_167245.1:g.2897351C>A	NT_167245.1:g.2897351=	NT_167245.1:g.2897351C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.2943284C>T	NT_167249.2:g.2943284C>A	NT_167249.2:g.2943284=	NT_167249.2:g.2943284C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.2942582C>T	NT_167249.1:g.2942582C>A	NT_167249.1:g.2942582=	NT_167249.1:g.2942582C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2949046C>T	NT_167246.2:g.2949046C>A	NT_167246.2:g.2949046=	NT_167246.2:g.2949046C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2954666C>T	NT_167246.1:g.2954666C>A	NT_167246.1:g.2954666=	NT_167246.1:g.2954666C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.2985865C>T	NT_167247.2:g.2985865C>A	NT_167247.2:g.2985865=	NT_167247.2:g.2985865C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.2991450C>T	NT_167247.1:g.2991450C>A	NT_167247.1:g.2991450=	NT_167247.1:g.2991450C>G
BAG6 transcript variant 4	NM_001098534.1:c.1561-23=	NM_001098534.1:c.1561-23A>T	NM_001098534.1:c.1561-23A>G	NM_001098534.1:c.1561-23A>C
BAG6 transcript variant 4	NM_001098534.2:c.1561-23=	NM_001098534.2:c.1561-23A>T	NM_001098534.2:c.1561-23A>G	NM_001098534.2:c.1561-23A>C
BAG6 transcript variant 5	NM_001199697.1:c.1561-26=	NM_001199697.1:c.1561-26A>T	NM_001199697.1:c.1561-26A>G	NM_001199697.1:c.1561-26A>C
BAG6 transcript variant 5	NM_001199697.2:c.1561-26=	NM_001199697.2:c.1561-26A>T	NM_001199697.2:c.1561-26A>G	NM_001199697.2:c.1561-26A>C
BAG6 transcript variant 6	NM_001199698.1:c.1561-23=	NM_001199698.1:c.1561-23A>T	NM_001199698.1:c.1561-23A>G	NM_001199698.1:c.1561-23A>C
BAG6 transcript variant 6	NM_001199698.2:c.1561-23=	NM_001199698.2:c.1561-23A>T	NM_001199698.2:c.1561-23A>G	NM_001199698.2:c.1561-23A>C
BAG6 transcript variant 7	NM_001387940.1:c.1561-23=	NM_001387940.1:c.1561-23A>T	NM_001387940.1:c.1561-23A>G	NM_001387940.1:c.1561-23A>C
BAG6 transcript variant 8	NM_001387942.1:c.1507-26=	NM_001387942.1:c.1507-26A>T	NM_001387942.1:c.1507-26A>G	NM_001387942.1:c.1507-26A>C
BAG6 transcript variant 9	NM_001387943.1:c.1669-23=	NM_001387943.1:c.1669-23A>T	NM_001387943.1:c.1669-23A>G	NM_001387943.1:c.1669-23A>C
BAG6 transcript variant 10	NM_001387944.1:c.1507-23=	NM_001387944.1:c.1507-23A>T	NM_001387944.1:c.1507-23A>G	NM_001387944.1:c.1507-23A>C
BAG6 transcript variant 11	NM_001387946.1:c.1669-23=	NM_001387946.1:c.1669-23A>T	NM_001387946.1:c.1669-23A>G	NM_001387946.1:c.1669-23A>C
BAG6 transcript variant 12	NM_001387949.1:c.1561-26=	NM_001387949.1:c.1561-26A>T	NM_001387949.1:c.1561-26A>G	NM_001387949.1:c.1561-26A>C
BAG6 transcript variant 13	NM_001387951.1:c.1561-23=	NM_001387951.1:c.1561-23A>T	NM_001387951.1:c.1561-23A>G	NM_001387951.1:c.1561-23A>C
BAG6 transcript variant 14	NM_001387954.1:c.1669-23=	NM_001387954.1:c.1669-23A>T	NM_001387954.1:c.1669-23A>G	NM_001387954.1:c.1669-23A>C
BAG6 transcript variant 15	NM_001387955.1:c.1561-26=	NM_001387955.1:c.1561-26A>T	NM_001387955.1:c.1561-26A>G	NM_001387955.1:c.1561-26A>C
BAG6 transcript variant 16	NM_001387956.1:c.1561-23=	NM_001387956.1:c.1561-23A>T	NM_001387956.1:c.1561-23A>G	NM_001387956.1:c.1561-23A>C
BAG6 transcript variant 17	NM_001387958.1:c.1615-23=	NM_001387958.1:c.1615-23A>T	NM_001387958.1:c.1615-23A>G	NM_001387958.1:c.1615-23A>C
BAG6 transcript variant 18	NM_001387961.1:c.1561-23=	NM_001387961.1:c.1561-23A>T	NM_001387961.1:c.1561-23A>G	NM_001387961.1:c.1561-23A>C
BAG6 transcript variant 19	NM_001387963.1:c.1507-26=	NM_001387963.1:c.1507-26A>T	NM_001387963.1:c.1507-26A>G	NM_001387963.1:c.1507-26A>C
BAG6 transcript variant 20	NM_001387964.1:c.1507-23=	NM_001387964.1:c.1507-23A>T	NM_001387964.1:c.1507-23A>G	NM_001387964.1:c.1507-23A>C
BAG6 transcript variant 21	NM_001387965.1:c.1669-23=	NM_001387965.1:c.1669-23A>T	NM_001387965.1:c.1669-23A>G	NM_001387965.1:c.1669-23A>C
BAG6 transcript variant 22	NM_001387982.1:c.1507-23=	NM_001387982.1:c.1507-23A>T	NM_001387982.1:c.1507-23A>G	NM_001387982.1:c.1507-23A>C
BAG6 transcript variant 23	NM_001387983.1:c.1669-26=	NM_001387983.1:c.1669-26A>T	NM_001387983.1:c.1669-26A>G	NM_001387983.1:c.1669-26A>C
BAG6 transcript variant 24	NM_001387984.1:c.1669-23=	NM_001387984.1:c.1669-23A>T	NM_001387984.1:c.1669-23A>G	NM_001387984.1:c.1669-23A>C
BAG6 transcript variant 25	NM_001387985.1:c.1696-23=	NM_001387985.1:c.1696-23A>T	NM_001387985.1:c.1696-23A>G	NM_001387985.1:c.1696-23A>C
BAG6 transcript variant 26	NM_001387986.1:c.1561-23=	NM_001387986.1:c.1561-23A>T	NM_001387986.1:c.1561-23A>G	NM_001387986.1:c.1561-23A>C
BAG6 transcript variant 27	NM_001387987.1:c.1561-26=	NM_001387987.1:c.1561-26A>T	NM_001387987.1:c.1561-26A>G	NM_001387987.1:c.1561-26A>C
BAG6 transcript variant 28	NM_001387988.1:c.1669-26=	NM_001387988.1:c.1669-26A>T	NM_001387988.1:c.1669-26A>G	NM_001387988.1:c.1669-26A>C
BAG6 transcript variant 29	NM_001387989.1:c.1669-23=	NM_001387989.1:c.1669-23A>T	NM_001387989.1:c.1669-23A>G	NM_001387989.1:c.1669-23A>C
BAG6 transcript variant 30	NM_001387990.1:c.1561-26=	NM_001387990.1:c.1561-26A>T	NM_001387990.1:c.1561-26A>G	NM_001387990.1:c.1561-26A>C
BAG6 transcript variant 31	NM_001387991.1:c.1615-23=	NM_001387991.1:c.1615-23A>T	NM_001387991.1:c.1615-23A>G	NM_001387991.1:c.1615-23A>C
BAG6 transcript variant 32	NM_001387992.1:c.1615-23=	NM_001387992.1:c.1615-23A>T	NM_001387992.1:c.1615-23A>G	NM_001387992.1:c.1615-23A>C
BAG6 transcript variant 33	NM_001387993.1:c.1669-26=	NM_001387993.1:c.1669-26A>T	NM_001387993.1:c.1669-26A>G	NM_001387993.1:c.1669-26A>C
BAG6 transcript variant 34	NM_001387994.1:c.1669-23=	NM_001387994.1:c.1669-23A>T	NM_001387994.1:c.1669-23A>G	NM_001387994.1:c.1669-23A>C
BAG6 transcript variant 35	NM_001387995.1:c.1669-26=	NM_001387995.1:c.1669-26A>T	NM_001387995.1:c.1669-26A>G	NM_001387995.1:c.1669-26A>C
BAG6 transcript variant 36	NM_001387996.1:c.1669-23=	NM_001387996.1:c.1669-23A>T	NM_001387996.1:c.1669-23A>G	NM_001387996.1:c.1669-23A>C
BAG6 transcript variant 37	NM_001387997.1:c.1507-23=	NM_001387997.1:c.1507-23A>T	NM_001387997.1:c.1507-23A>G	NM_001387997.1:c.1507-23A>C
BAG6 transcript variant 38	NM_001387998.1:c.1561-26=	NM_001387998.1:c.1561-26A>T	NM_001387998.1:c.1561-26A>G	NM_001387998.1:c.1561-26A>C
BAG6 transcript variant 39	NM_001387999.1:c.1561-23=	NM_001387999.1:c.1561-23A>T	NM_001387999.1:c.1561-23A>G	NM_001387999.1:c.1561-23A>C
BAG6 transcript variant 40	NM_001388000.1:c.1561-26=	NM_001388000.1:c.1561-26A>T	NM_001388000.1:c.1561-26A>G	NM_001388000.1:c.1561-26A>C
BAG6 transcript variant 41	NM_001388001.1:c.1561-23=	NM_001388001.1:c.1561-23A>T	NM_001388001.1:c.1561-23A>G	NM_001388001.1:c.1561-23A>C
BAG6 transcript variant 42	NM_001388002.1:c.1483-26=	NM_001388002.1:c.1483-26A>T	NM_001388002.1:c.1483-26A>G	NM_001388002.1:c.1483-26A>C
BAG6 transcript variant 43	NM_001388003.1:c.1483-23=	NM_001388003.1:c.1483-23A>T	NM_001388003.1:c.1483-23A>G	NM_001388003.1:c.1483-23A>C
BAG6 transcript variant 44	NM_001388004.1:c.1507-23=	NM_001388004.1:c.1507-23A>T	NM_001388004.1:c.1507-23A>G	NM_001388004.1:c.1507-23A>C
BAG6 transcript variant 45	NM_001388005.1:c.1669-26=	NM_001388005.1:c.1669-26A>T	NM_001388005.1:c.1669-26A>G	NM_001388005.1:c.1669-26A>C
BAG6 transcript variant 46	NM_001388006.1:c.1669-23=	NM_001388006.1:c.1669-23A>T	NM_001388006.1:c.1669-23A>G	NM_001388006.1:c.1669-23A>C
BAG6 transcript variant 47	NM_001388007.1:c.1561-26=	NM_001388007.1:c.1561-26A>T	NM_001388007.1:c.1561-26A>G	NM_001388007.1:c.1561-26A>C
BAG6 transcript variant 48	NM_001388008.1:c.1588-26=	NM_001388008.1:c.1588-26A>T	NM_001388008.1:c.1588-26A>G	NM_001388008.1:c.1588-26A>C
BAG6 transcript variant 49	NM_001388009.1:c.1588-23=	NM_001388009.1:c.1588-23A>T	NM_001388009.1:c.1588-23A>G	NM_001388009.1:c.1588-23A>C
BAG6 transcript variant 50	NM_001388010.1:c.1669-26=	NM_001388010.1:c.1669-26A>T	NM_001388010.1:c.1669-26A>G	NM_001388010.1:c.1669-26A>C
BAG6 transcript variant 51	NM_001388011.1:c.1669-23=	NM_001388011.1:c.1669-23A>T	NM_001388011.1:c.1669-23A>G	NM_001388011.1:c.1669-23A>C
BAG6 transcript variant 52	NM_001388012.1:c.1696-23=	NM_001388012.1:c.1696-23A>T	NM_001388012.1:c.1696-23A>G	NM_001388012.1:c.1696-23A>C
BAG6 transcript variant 53	NM_001388013.1:c.1507-26=	NM_001388013.1:c.1507-26A>T	NM_001388013.1:c.1507-26A>G	NM_001388013.1:c.1507-26A>C
BAG6 transcript variant 54	NM_001388014.1:c.1561-23=	NM_001388014.1:c.1561-23A>T	NM_001388014.1:c.1561-23A>G	NM_001388014.1:c.1561-23A>C
BAG6 transcript variant 55	NM_001388015.1:c.1561-23=	NM_001388015.1:c.1561-23A>T	NM_001388015.1:c.1561-23A>G	NM_001388015.1:c.1561-23A>C
BAG6 transcript variant 56	NM_001388016.1:c.1669-26=	NM_001388016.1:c.1669-26A>T	NM_001388016.1:c.1669-26A>G	NM_001388016.1:c.1669-26A>C
BAG6 transcript variant 57	NM_001388017.1:c.1561-23=	NM_001388017.1:c.1561-23A>T	NM_001388017.1:c.1561-23A>G	NM_001388017.1:c.1561-23A>C
BAG6 transcript variant 58	NM_001388018.1:c.1561-23=	NM_001388018.1:c.1561-23A>T	NM_001388018.1:c.1561-23A>G	NM_001388018.1:c.1561-23A>C
BAG6 transcript variant 59	NM_001388019.1:c.1669-26=	NM_001388019.1:c.1669-26A>T	NM_001388019.1:c.1669-26A>G	NM_001388019.1:c.1669-26A>C
BAG6 transcript variant 60	NM_001388020.1:c.1669-23=	NM_001388020.1:c.1669-23A>T	NM_001388020.1:c.1669-23A>G	NM_001388020.1:c.1669-23A>C
BAG6 transcript variant 1	NM_004639.3:c.1579-23=	NM_004639.3:c.1579-23A>T	NM_004639.3:c.1579-23A>G	NM_004639.3:c.1579-23A>C
BAG6 transcript variant 2	NM_080702.2:c.1561-23=	NM_080702.2:c.1561-23A>T	NM_080702.2:c.1561-23A>G	NM_080702.2:c.1561-23A>C
BAG6 transcript variant 2	NM_080702.3:c.1561-23=	NM_080702.3:c.1561-23A>T	NM_080702.3:c.1561-23A>G	NM_080702.3:c.1561-23A>C
BAG6 transcript variant 3	NM_080703.2:c.1561-23=	NM_080703.2:c.1561-23A>T	NM_080703.2:c.1561-23A>G	NM_080703.2:c.1561-23A>C
BAG6 transcript variant 3	NM_080703.3:c.1561-23=	NM_080703.3:c.1561-23A>T	NM_080703.3:c.1561-23A>G	NM_080703.3:c.1561-23A>C
BAG6 transcript variant X1	XM_005249393.1:c.1669-23=	XM_005249393.1:c.1669-23A>T	XM_005249393.1:c.1669-23A>G	XM_005249393.1:c.1669-23A>C
BAG6 transcript variant X2	XM_005249394.1:c.1669-23=	XM_005249394.1:c.1669-23A>T	XM_005249394.1:c.1669-23A>G	XM_005249394.1:c.1669-23A>C
BAG6 transcript variant X3	XM_005249395.1:c.1669-26=	XM_005249395.1:c.1669-26A>T	XM_005249395.1:c.1669-26A>G	XM_005249395.1:c.1669-26A>C
BAG6 transcript variant X4	XM_005249396.1:c.1615-23=	XM_005249396.1:c.1615-23A>T	XM_005249396.1:c.1615-23A>G	XM_005249396.1:c.1615-23A>C
BAG6 transcript variant X5	XM_005249397.1:c.1603-23=	XM_005249397.1:c.1603-23A>T	XM_005249397.1:c.1603-23A>G	XM_005249397.1:c.1603-23A>C
BAG6 transcript variant X6	XM_005249398.1:c.1561-26=	XM_005249398.1:c.1561-26A>T	XM_005249398.1:c.1561-26A>G	XM_005249398.1:c.1561-26A>C
BAG6 transcript variant X7	XM_005249399.1:c.1669-23=	XM_005249399.1:c.1669-23A>T	XM_005249399.1:c.1669-23A>G	XM_005249399.1:c.1669-23A>C
BAG6 transcript variant X8	XM_005249400.1:c.1561-26=	XM_005249400.1:c.1561-26A>T	XM_005249400.1:c.1561-26A>G	XM_005249400.1:c.1561-26A>C
BAG6 transcript variant X9	XM_005249401.1:c.1669-23=	XM_005249401.1:c.1669-23A>T	XM_005249401.1:c.1669-23A>G	XM_005249401.1:c.1669-23A>C
BAG6 transcript variant X1	XM_005272880.1:c.1669-23G>A	XM_005272880.1:c.1669-23G>T	XM_005272880.1:c.1669-23=	XM_005272880.1:c.1669-23G>C
BAG6 transcript variant X2	XM_005272881.1:c.1669-23G>A	XM_005272881.1:c.1669-23G>T	XM_005272881.1:c.1669-23=	XM_005272881.1:c.1669-23G>C
BAG6 transcript variant X3	XM_005272882.1:c.1669-26G>A	XM_005272882.1:c.1669-26G>T	XM_005272882.1:c.1669-26=	XM_005272882.1:c.1669-26G>C
BAG6 transcript variant X4	XM_005272883.1:c.1615-23G>A	XM_005272883.1:c.1615-23G>T	XM_005272883.1:c.1615-23=	XM_005272883.1:c.1615-23G>C
BAG6 transcript variant X5	XM_005272884.1:c.1603-23G>A	XM_005272884.1:c.1603-23G>T	XM_005272884.1:c.1603-23=	XM_005272884.1:c.1603-23G>C
BAG6 transcript variant X6	XM_005272885.1:c.1561-26G>A	XM_005272885.1:c.1561-26G>T	XM_005272885.1:c.1561-26=	XM_005272885.1:c.1561-26G>C
BAG6 transcript variant X7	XM_005272886.1:c.1669-23G>A	XM_005272886.1:c.1669-23G>T	XM_005272886.1:c.1669-23=	XM_005272886.1:c.1669-23G>C
BAG6 transcript variant X8	XM_005272887.1:c.1561-26G>A	XM_005272887.1:c.1561-26G>T	XM_005272887.1:c.1561-26=	XM_005272887.1:c.1561-26G>C
BAG6 transcript variant X9	XM_005272888.1:c.1669-23G>A	XM_005272888.1:c.1669-23G>T	XM_005272888.1:c.1669-23=	XM_005272888.1:c.1669-23G>C
BAG6 transcript variant X1	XM_005275034.1:c.1669-23G>A	XM_005275034.1:c.1669-23G>T	XM_005275034.1:c.1669-23=	XM_005275034.1:c.1669-23G>C
BAG6 transcript variant X2	XM_005275035.1:c.1669-23G>A	XM_005275035.1:c.1669-23G>T	XM_005275035.1:c.1669-23=	XM_005275035.1:c.1669-23G>C
BAG6 transcript variant X3	XM_005275036.1:c.1669-26G>A	XM_005275036.1:c.1669-26G>T	XM_005275036.1:c.1669-26=	XM_005275036.1:c.1669-26G>C
BAG6 transcript variant X4	XM_005275037.1:c.1615-23G>A	XM_005275037.1:c.1615-23G>T	XM_005275037.1:c.1615-23=	XM_005275037.1:c.1615-23G>C
BAG6 transcript variant X5	XM_005275038.1:c.1603-23G>A	XM_005275038.1:c.1603-23G>T	XM_005275038.1:c.1603-23=	XM_005275038.1:c.1603-23G>C
BAG6 transcript variant X6	XM_005275039.1:c.1561-26G>A	XM_005275039.1:c.1561-26G>T	XM_005275039.1:c.1561-26=	XM_005275039.1:c.1561-26G>C
BAG6 transcript variant X7	XM_005275040.1:c.1669-23G>A	XM_005275040.1:c.1669-23G>T	XM_005275040.1:c.1669-23=	XM_005275040.1:c.1669-23G>C
BAG6 transcript variant X8	XM_005275041.1:c.1561-26G>A	XM_005275041.1:c.1561-26G>T	XM_005275041.1:c.1561-26=	XM_005275041.1:c.1561-26G>C
BAG6 transcript variant X9	XM_005275042.1:c.1669-23G>A	XM_005275042.1:c.1669-23G>T	XM_005275042.1:c.1669-23=	XM_005275042.1:c.1669-23G>C
BAG6 transcript variant X1	XM_005275169.1:c.1669-23G>A	XM_005275169.1:c.1669-23G>T	XM_005275169.1:c.1669-23=	XM_005275169.1:c.1669-23G>C
BAG6 transcript variant X2	XM_005275170.1:c.1669-23G>A	XM_005275170.1:c.1669-23G>T	XM_005275170.1:c.1669-23=	XM_005275170.1:c.1669-23G>C
BAG6 transcript variant X3	XM_005275171.1:c.1669-26G>A	XM_005275171.1:c.1669-26G>T	XM_005275171.1:c.1669-26=	XM_005275171.1:c.1669-26G>C
BAG6 transcript variant X4	XM_005275172.1:c.1615-23G>A	XM_005275172.1:c.1615-23G>T	XM_005275172.1:c.1615-23=	XM_005275172.1:c.1615-23G>C
BAG6 transcript variant X5	XM_005275173.1:c.1603-23G>A	XM_005275173.1:c.1603-23G>T	XM_005275173.1:c.1603-23=	XM_005275173.1:c.1603-23G>C
BAG6 transcript variant X6	XM_005275174.1:c.1561-26G>A	XM_005275174.1:c.1561-26G>T	XM_005275174.1:c.1561-26=	XM_005275174.1:c.1561-26G>C
BAG6 transcript variant X7	XM_005275175.1:c.1669-23G>A	XM_005275175.1:c.1669-23G>T	XM_005275175.1:c.1669-23=	XM_005275175.1:c.1669-23G>C
BAG6 transcript variant X8	XM_005275176.1:c.1561-26G>A	XM_005275176.1:c.1561-26G>T	XM_005275176.1:c.1561-26=	XM_005275176.1:c.1561-26G>C
BAG6 transcript variant X9	XM_005275177.1:c.1669-23G>A	XM_005275177.1:c.1669-23G>T	XM_005275177.1:c.1669-23=	XM_005275177.1:c.1669-23G>C
BAG6 transcript variant X1	XM_005275292.1:c.1669-23G>A	XM_005275292.1:c.1669-23G>T	XM_005275292.1:c.1669-23=	XM_005275292.1:c.1669-23G>C
BAG6 transcript variant X2	XM_005275293.1:c.1669-23G>A	XM_005275293.1:c.1669-23G>T	XM_005275293.1:c.1669-23=	XM_005275293.1:c.1669-23G>C
BAG6 transcript variant X3	XM_005275294.1:c.1669-26G>A	XM_005275294.1:c.1669-26G>T	XM_005275294.1:c.1669-26=	XM_005275294.1:c.1669-26G>C
BAG6 transcript variant X4	XM_005275295.1:c.1615-23G>A	XM_005275295.1:c.1615-23G>T	XM_005275295.1:c.1615-23=	XM_005275295.1:c.1615-23G>C
BAG6 transcript variant X5	XM_005275296.1:c.1603-23G>A	XM_005275296.1:c.1603-23G>T	XM_005275296.1:c.1603-23=	XM_005275296.1:c.1603-23G>C
BAG6 transcript variant X6	XM_005275297.1:c.1561-26G>A	XM_005275297.1:c.1561-26G>T	XM_005275297.1:c.1561-26=	XM_005275297.1:c.1561-26G>C
BAG6 transcript variant X7	XM_005275298.1:c.1669-23G>A	XM_005275298.1:c.1669-23G>T	XM_005275298.1:c.1669-23=	XM_005275298.1:c.1669-23G>C
BAG6 transcript variant X8	XM_005275299.1:c.1561-26G>A	XM_005275299.1:c.1561-26G>T	XM_005275299.1:c.1561-26=	XM_005275299.1:c.1561-26G>C
BAG6 transcript variant X9	XM_005275300.1:c.1669-23G>A	XM_005275300.1:c.1669-23G>T	XM_005275300.1:c.1669-23=	XM_005275300.1:c.1669-23G>C
BAG6 transcript variant X1	XM_005275464.1:c.1669-23G>A	XM_005275464.1:c.1669-23G>T	XM_005275464.1:c.1669-23=	XM_005275464.1:c.1669-23G>C
BAG6 transcript variant X2	XM_005275465.1:c.1669-23G>A	XM_005275465.1:c.1669-23G>T	XM_005275465.1:c.1669-23=	XM_005275465.1:c.1669-23G>C
BAG6 transcript variant X3	XM_005275466.1:c.1669-23G>A	XM_005275466.1:c.1669-23G>T	XM_005275466.1:c.1669-23=	XM_005275466.1:c.1669-23G>C
BAG6 transcript variant X4	XM_005275467.1:c.1669-26G>A	XM_005275467.1:c.1669-26G>T	XM_005275467.1:c.1669-26=	XM_005275467.1:c.1669-26G>C
BAG6 transcript variant X5	XM_005275468.1:c.1615-23G>A	XM_005275468.1:c.1615-23G>T	XM_005275468.1:c.1615-23=	XM_005275468.1:c.1615-23G>C
BAG6 transcript variant X6	XM_005275469.1:c.1603-23G>A	XM_005275469.1:c.1603-23G>T	XM_005275469.1:c.1603-23=	XM_005275469.1:c.1603-23G>C
BAG6 transcript variant X7	XM_005275470.1:c.1561-26G>A	XM_005275470.1:c.1561-26G>T	XM_005275470.1:c.1561-26=	XM_005275470.1:c.1561-26G>C
BAG6 transcript variant X8	XM_005275471.1:c.1669-23G>A	XM_005275471.1:c.1669-23G>T	XM_005275471.1:c.1669-23=	XM_005275471.1:c.1669-23G>C
BAG6 transcript variant X9	XM_005275472.1:c.1561-26G>A	XM_005275472.1:c.1561-26G>T	XM_005275472.1:c.1561-26=	XM_005275472.1:c.1561-26G>C
BAG6 transcript variant X10	XM_005275473.1:c.1669-23G>A	XM_005275473.1:c.1669-23G>T	XM_005275473.1:c.1669-23=	XM_005275473.1:c.1669-23G>C
BAG6 transcript variant X1	XM_005275597.1:c.1669-23G>A	XM_005275597.1:c.1669-23G>T	XM_005275597.1:c.1669-23=	XM_005275597.1:c.1669-23G>C
BAG6 transcript variant X2	XM_005275598.1:c.1669-23G>A	XM_005275598.1:c.1669-23G>T	XM_005275598.1:c.1669-23=	XM_005275598.1:c.1669-23G>C
BAG6 transcript variant X3	XM_005275599.1:c.1669-23G>A	XM_005275599.1:c.1669-23G>T	XM_005275599.1:c.1669-23=	XM_005275599.1:c.1669-23G>C
BAG6 transcript variant X4	XM_005275600.1:c.1669-26G>A	XM_005275600.1:c.1669-26G>T	XM_005275600.1:c.1669-26=	XM_005275600.1:c.1669-26G>C
BAG6 transcript variant X5	XM_005275601.1:c.1615-23G>A	XM_005275601.1:c.1615-23G>T	XM_005275601.1:c.1615-23=	XM_005275601.1:c.1615-23G>C
BAG6 transcript variant X6	XM_005275602.1:c.1603-23G>A	XM_005275602.1:c.1603-23G>T	XM_005275602.1:c.1603-23=	XM_005275602.1:c.1603-23G>C
BAG6 transcript variant X7	XM_005275603.1:c.1561-26G>A	XM_005275603.1:c.1561-26G>T	XM_005275603.1:c.1561-26=	XM_005275603.1:c.1561-26G>C
BAG6 transcript variant X8	XM_005275604.1:c.1669-23G>A	XM_005275604.1:c.1669-23G>T	XM_005275604.1:c.1669-23=	XM_005275604.1:c.1669-23G>C
BAG6 transcript variant X9	XM_005275605.1:c.1561-26G>A	XM_005275605.1:c.1561-26G>T	XM_005275605.1:c.1561-26=	XM_005275605.1:c.1561-26G>C
BAG6 transcript variant X10	XM_005275606.1:c.1669-23G>A	XM_005275606.1:c.1669-23G>T	XM_005275606.1:c.1669-23=	XM_005275606.1:c.1669-23G>C
BAG6 transcript variant X12	XM_017011296.2:c.1561-26=	XM_017011296.2:c.1561-26A>T	XM_017011296.2:c.1561-26A>G	XM_017011296.2:c.1561-26A>C
BAG6 transcript variant X9	XM_017011297.2:c.1615-26=	XM_017011297.2:c.1615-26A>T	XM_017011297.2:c.1615-26A>G	XM_017011297.2:c.1615-26A>C
BAG6 transcript variant X1	XM_047419338.1:c.1615-23=	XM_047419338.1:c.1615-23A>T	XM_047419338.1:c.1615-23A>G	XM_047419338.1:c.1615-23A>C
BAG6 transcript variant X2	XM_047419339.1:c.1615-26=	XM_047419339.1:c.1615-26A>T	XM_047419339.1:c.1615-26A>G	XM_047419339.1:c.1615-26A>C
BAG6 transcript variant X3	XM_047419340.1:c.1615-26=	XM_047419340.1:c.1615-26A>T	XM_047419340.1:c.1615-26A>G	XM_047419340.1:c.1615-26A>C
BAG6 transcript variant X4	XM_047419341.1:c.1669-26=	XM_047419341.1:c.1669-26A>T	XM_047419341.1:c.1669-26A>G	XM_047419341.1:c.1669-26A>C
BAG6 transcript variant X5	XM_047419342.1:c.1507-26=	XM_047419342.1:c.1507-26A>T	XM_047419342.1:c.1507-26A>G	XM_047419342.1:c.1507-26A>C
BAG6 transcript variant X6	XM_047419343.1:c.1507-26=	XM_047419343.1:c.1507-26A>T	XM_047419343.1:c.1507-26A>G	XM_047419343.1:c.1507-26A>C
BAG6 transcript variant X7	XM_047419344.1:c.1615-23=	XM_047419344.1:c.1615-23A>T	XM_047419344.1:c.1615-23A>G	XM_047419344.1:c.1615-23A>C
BAG6 transcript variant X8	XM_047419345.1:c.1615-23=	XM_047419345.1:c.1615-23A>T	XM_047419345.1:c.1615-23A>G	XM_047419345.1:c.1615-23A>C
BAG6 transcript variant X10	XM_047419346.1:c.1615-26=	XM_047419346.1:c.1615-26A>T	XM_047419346.1:c.1615-26A>G	XM_047419346.1:c.1615-26A>C
BAG6 transcript variant X11	XM_047419347.1:c.1615-26=	XM_047419347.1:c.1615-26A>T	XM_047419347.1:c.1615-26A>G	XM_047419347.1:c.1615-26A>C
BAG6 transcript variant X13	XM_047419348.1:c.1507-23=	XM_047419348.1:c.1507-23A>T	XM_047419348.1:c.1507-23A>G	XM_047419348.1:c.1507-23A>C
BAG6 transcript variant X14	XM_047419349.1:c.1507-26=	XM_047419349.1:c.1507-26A>T	XM_047419349.1:c.1507-26A>G	XM_047419349.1:c.1507-26A>C

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

146 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss133122	Oct 05, 2000 (86)
2	YUSUKE	ss3199053	Aug 15, 2001 (98)
3	SC_JCM	ss4377962	Mar 26, 2002 (103)
4	WI_SSAHASNP	ss11797655	Jul 11, 2003 (117)
5	SI_MHC_SNP	ss12691574	Oct 31, 2003 (118)
6	CSHL-HAPMAP	ss17107920	Feb 27, 2004 (120)
7	CSHL-HAPMAP	ss19659647	Feb 27, 2004 (120)
8	SSAHASNP	ss22424818	Apr 05, 2004 (121)
9	FHCRC	ss23137850	Sep 20, 2004 (126)
10	KRIBB_YJKIM	ss65842182	Dec 01, 2006 (127)
11	AFFY	ss66139199	Dec 01, 2006 (127)
12	SI_EXO	ss71644732	May 17, 2007 (127)
13	AFFY	ss76155047	Dec 08, 2007 (129)
14	KRIBB_YJKIM	ss81436843	Dec 14, 2007 (130)
15	HGSV	ss82026491	Dec 16, 2007 (130)
16	BCMHGSC_JDW	ss93436594	Mar 24, 2008 (129)
17	HUMANGENOME_JCVI	ss98379899	Feb 06, 2009 (130)
18	BGI	ss105991228	Feb 06, 2009 (130)
19	1000GENOMES	ss109902075	Feb 13, 2009 (136)
20	1000GENOMES	ss114145310	Jan 25, 2009 (136)
21	ILLUMINA-UK	ss116394915	Feb 14, 2009 (130)
22	ENSEMBL	ss139847526	Dec 01, 2009 (131)
23	GMI	ss156748345	Dec 01, 2009 (131)
24	ILLUMINA	ss160893921	Dec 01, 2009 (131)
25	COMPLETE_GENOMICS	ss162199039	Jul 04, 2010 (132)
26	COMPLETE_GENOMICS	ss163348736	Jul 04, 2010 (132)
27	COMPLETE_GENOMICS	ss166429832	Jul 04, 2010 (132)
28	AFFY	ss172659174	Jul 04, 2010 (132)
29	BUSHMAN	ss201626625	Jul 04, 2010 (132)
30	BCM-HGSC-SUB	ss207357473	Jul 04, 2010 (132)
31	1000GENOMES	ss222304354	Jul 14, 2010 (136)
32	1000GENOMES	ss233399403	Jul 14, 2010 (136)
33	1000GENOMES	ss240470077	Jul 15, 2010 (136)
34	BL	ss254187877	May 09, 2011 (136)
35	GMI	ss278727312	May 04, 2012 (137)
36	GMI	ss285374243	Apr 25, 2013 (138)
37	PJP	ss293826052	May 09, 2011 (136)
38	ILLUMINA	ss482610626	Sep 08, 2015 (146)
39	EXOME_CHIP	ss491382040	May 04, 2012 (137)
40	ILLUMINA	ss537489160	Sep 08, 2015 (146)
41	TISHKOFF	ss559114621	Apr 25, 2013 (138)
42	SSMP	ss653035972	Apr 25, 2013 (138)
43	NHLBI-ESP	ss712699548	Apr 25, 2013 (138)
44	ILLUMINA	ss778712159	Sep 08, 2015 (146)
45	ILLUMINA	ss780686645	Sep 08, 2015 (146)
46	ILLUMINA	ss783360173	Sep 08, 2015 (146)
47	ILLUMINA	ss834171340	Sep 08, 2015 (146)
48	EVA-GONL	ss982767027	Aug 21, 2014 (142)
49	JMKIDD_LAB	ss1073506391	Aug 21, 2014 (142)
50	1000GENOMES	ss1319560818	Aug 21, 2014 (142)
51	EVA_GENOME_DK	ss1581607060	Apr 01, 2015 (144)
52	EVA_DECODE	ss1592310893	Apr 01, 2015 (144)
53	EVA_UK10K_ALSPAC	ss1615279021	Apr 01, 2015 (144)
54	EVA_UK10K_TWINSUK	ss1658273054	Apr 01, 2015 (144)
55	EVA_EXAC	ss1688234054	Apr 01, 2015 (144)
56	EVA_MGP	ss1711121321	Apr 01, 2015 (144)
57	EVA_SVP	ss1712851179	Apr 01, 2015 (144)
58	HAMMER_LAB	ss1804358574	Sep 08, 2015 (146)
59	ILLUMINA	ss1917802563	Feb 12, 2016 (147)
60	WEILL_CORNELL_DGM	ss1926019298	Feb 12, 2016 (147)
61	ILLUMINA	ss1946173502	Feb 12, 2016 (147)
62	ILLUMINA	ss1958888755	Feb 12, 2016 (147)
63	GENOMED	ss1970357702	Jul 19, 2016 (147)
64	JJLAB	ss2023642882	Sep 14, 2016 (149)
65	ILLUMINA	ss2094824903	Dec 20, 2016 (150)
66	ILLUMINA	ss2095178145	Dec 20, 2016 (150)
67	USC_VALOUEV	ss2151809414	Dec 20, 2016 (150)
68	HUMAN_LONGEVITY	ss2282950019	Dec 20, 2016 (150)
69	SYSTEMSBIOZJU	ss2626308899	Nov 08, 2017 (151)
70	ILLUMINA	ss2634430230	Nov 08, 2017 (151)
71	GRF	ss2707403220	Nov 08, 2017 (151)
72	ILLUMINA	ss2711069679	Nov 08, 2017 (151)
73	GNOMAD	ss2735653856	Nov 08, 2017 (151)
74	GNOMAD	ss2747583156	Nov 08, 2017 (151)
75	AFFY	ss2985362465	Nov 08, 2017 (151)
76	AFFY	ss2985994335	Nov 08, 2017 (151)
77	SWEGEN	ss2998797427	Nov 08, 2017 (151)
78	ILLUMINA	ss3022599916	Nov 08, 2017 (151)
79	BIOINF_KMB_FNS_UNIBA	ss3025608573	Nov 08, 2017 (151)
80	CSHL	ss3346902340	Nov 08, 2017 (151)
81	ILLUMINA	ss3629504133	Oct 12, 2018 (152)
82	ILLUMINA	ss3629504134	Oct 12, 2018 (152)
83	ILLUMINA	ss3632348741	Oct 12, 2018 (152)
84	ILLUMINA	ss3635057251	Oct 12, 2018 (152)
85	ILLUMINA	ss3636778494	Oct 12, 2018 (152)
86	ILLUMINA	ss3640764550	Oct 12, 2018 (152)
87	ILLUMINA	ss3644906562	Oct 12, 2018 (152)
88	OMUKHERJEE_ADBS	ss3646334850	Oct 12, 2018 (152)
89	URBANLAB	ss3648310221	Oct 12, 2018 (152)
90	ILLUMINA	ss3653112593	Oct 12, 2018 (152)
91	ILLUMINA	ss3653112594	Oct 12, 2018 (152)
92	ILLUMINA	ss3654128248	Oct 12, 2018 (152)
93	EGCUT_WGS	ss3666711841	Jul 13, 2019 (153)
94	EVA_DECODE	ss3716910380	Jul 13, 2019 (153)
95	ILLUMINA	ss3726330387	Jul 13, 2019 (153)
96	ACPOP	ss3733362632	Jul 13, 2019 (153)
97	ILLUMINA	ss3744550015	Jul 13, 2019 (153)
98	ILLUMINA	ss3745357248	Jul 13, 2019 (153)
99	EVA	ss3764823712	Jul 13, 2019 (153)
100	PAGE_CC	ss3771279245	Jul 13, 2019 (153)
101	PACBIO	ss3785425927	Jul 13, 2019 (153)
102	PACBIO	ss3790785298	Jul 13, 2019 (153)
103	PACBIO	ss3795662816	Jul 13, 2019 (153)
104	KHV_HUMAN_GENOMES	ss3807978829	Jul 13, 2019 (153)
105	EVA	ss3824170770	Apr 26, 2020 (154)
106	EVA	ss3825694375	Apr 26, 2020 (154)
107	EVA	ss3829833357	Apr 26, 2020 (154)
108	EVA	ss3838395031	Apr 26, 2020 (154)
109	EVA	ss3843837220	Apr 26, 2020 (154)
110	SGDP_PRJ	ss3864256575	Apr 26, 2020 (154)
111	KRGDB	ss3911031803	Apr 26, 2020 (154)
112	FSA-LAB	ss3984333351	Apr 26, 2021 (155)
113	EVA	ss3984565782	Apr 26, 2021 (155)
114	EVA	ss3985213241	Apr 26, 2021 (155)
115	VINODS	ss4025188829	Apr 26, 2021 (155)
116	VINODS	ss4025209488	Apr 26, 2021 (155)
117	VINODS	ss4025229550	Apr 26, 2021 (155)
118	VINODS	ss4025248191	Apr 26, 2021 (155)
119	VINODS	ss4025266906	Apr 26, 2021 (155)
120	TOPMED	ss4698409801	Apr 26, 2021 (155)
121	TOMMO_GENOMICS	ss5176840346	Apr 26, 2021 (155)
122	EVA	ss5237190552	Apr 26, 2021 (155)
123	1000G_HIGH_COVERAGE	ss5267939296	Oct 17, 2022 (156)
124	EVA	ss5315142449	Oct 17, 2022 (156)
125	EVA	ss5364726791	Oct 17, 2022 (156)
126	HUGCELL_USP	ss5465672953	Oct 17, 2022 (156)
127	EVA	ss5508428939	Oct 17, 2022 (156)
128	1000G_HIGH_COVERAGE	ss5553596561	Oct 17, 2022 (156)
129	EVA	ss5623935748	Oct 17, 2022 (156)
130	SANFORD_IMAGENETICS	ss5624623903	Oct 17, 2022 (156)
131	SANFORD_IMAGENETICS	ss5640091137	Oct 17, 2022 (156)
132	TOMMO_GENOMICS	ss5714696356	Oct 17, 2022 (156)
133	EVA	ss5800055678	Oct 17, 2022 (156)
134	EVA	ss5800129075	Oct 17, 2022 (156)
135	YY_MCH	ss5807308483	Oct 17, 2022 (156)
136	EVA	ss5842028327	Oct 17, 2022 (156)
137	EVA	ss5847291071	Oct 17, 2022 (156)
138	EVA	ss5848089872	Oct 17, 2022 (156)
139	EVA	ss5848651544	Oct 17, 2022 (156)
140	EVA	ss5855284413	Oct 17, 2022 (156)
141	EVA	ss5883246748	Oct 17, 2022 (156)
142	EVA	ss5936530753	Oct 17, 2022 (156)
143	EVA	ss5968592985	Oct 17, 2022 (156)
144	EVA	ss5979780294	Oct 17, 2022 (156)
145	EVA	ss5980356802	Oct 17, 2022 (156)
146	EVA	ss5981234488	Oct 17, 2022 (156)
147	1000Genomes	NC_000006.11 - 31611777	Oct 12, 2018 (152)
148	1000Genomes_30x	NC_000006.12 - 31644000	Oct 17, 2022 (156)
149	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 31611777	Oct 12, 2018 (152)
150	Genetic variation in the Estonian population	NC_000006.11 - 31611777	Oct 12, 2018 (152)
151	ExAC	NC_000006.11 - 31611777	Oct 12, 2018 (152)
152	The Danish reference pan genome	NC_000006.11 - 31611777	Apr 26, 2020 (154)
153	gnomAD - Genomes	NC_000006.12 - 31644000	Apr 26, 2021 (155)
154	gnomAD - Exomes	NC_000006.11 - 31611777	Jul 13, 2019 (153)
155	GO Exome Sequencing Project	NC_000006.11 - 31611777	Oct 12, 2018 (152)
156	Genome of the Netherlands Release 5	NC_000006.11 - 31611777	Apr 26, 2020 (154)
157	KOREAN population from KRGDB	NC_000006.11 - 31611777	Apr 26, 2020 (154)
158	Medical Genome Project healthy controls from Spanish population	NC_000006.11 - 31611777	Apr 26, 2020 (154)
159	Northern Sweden	NC_000006.11 - 31611777	Jul 13, 2019 (153)
160	The PAGE Study	NC_000006.12 - 31644000	Jul 13, 2019 (153)
161	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000006.11 - 31611777	Apr 26, 2021 (155)
162	CNV burdens in cranial meningiomas	NC_000006.11 - 31611777	Apr 26, 2021 (155)
163	Qatari	NC_000006.11 - 31611777	Apr 26, 2020 (154)
164	SGDP_PRJ	NC_000006.11 - 31611777	Apr 26, 2020 (154)
165	Siberian	NC_000006.11 - 31611777	Apr 26, 2020 (154)
166	8.3KJPN	NC_000006.11 - 31611777	Apr 26, 2021 (155)
167	14KJPN	NC_000006.12 - 31644000	Oct 17, 2022 (156)
168	TopMed	NC_000006.12 - 31644000	Apr 26, 2021 (155)
169	UK 10K study - Twins	NC_000006.11 - 31611777	Oct 12, 2018 (152)
170	A Vietnamese Genetic Variation Database	NC_000006.11 - 31611777	Jul 13, 2019 (153)
171	ALFA	NC_000006.12 - 31644000	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs7752849	Aug 27, 2003 (117)
rs17200900	Mar 10, 2006 (126)
rs57061281	Feb 27, 2009 (130)
rs61341978	May 26, 2008 (130)
rs115159617	Mar 28, 2012 (136)
rs117168431	Aug 16, 2010 (132)
rs386611854	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
18209197, ss3911031803	NC_000006.11:31611776:T:A	NC_000006.12:31643999:T:A	(self)
ss82026491	NC_000006.9:31719755:T:C	NC_000006.12:31643999:T:C	(self)
ss66139199, ss76155047, ss93436594, ss109902075, ss114145310, ss116394915, ss162199039, ss163348736, ss166429832, ss172659174, ss201626625, ss207357473, ss254187877, ss278727312, ss285374243, ss293826052, ss1592310893, ss1712851179	NC_000006.10:31719755:T:C	NC_000006.12:31643999:T:C	(self)
31328353, 17468712, 12450089, 8259570, 7771999, 4796535, 628813, 7765778, 18209197, 237081, 6647497, 439168, 115186, 8061228, 16273555, 4325768, 34809653, 17468712, 3874019, ss222304354, ss233399403, ss240470077, ss482610626, ss491382040, ss537489160, ss559114621, ss653035972, ss712699548, ss778712159, ss780686645, ss783360173, ss834171340, ss982767027, ss1073506391, ss1319560818, ss1581607060, ss1615279021, ss1658273054, ss1688234054, ss1711121321, ss1804358574, ss1917802563, ss1926019298, ss1946173502, ss1958888755, ss1970357702, ss2023642882, ss2094824903, ss2095178145, ss2151809414, ss2626308899, ss2634430230, ss2707403220, ss2711069679, ss2735653856, ss2747583156, ss2985362465, ss2985994335, ss2998797427, ss3022599916, ss3346902340, ss3629504133, ss3629504134, ss3632348741, ss3635057251, ss3636778494, ss3640764550, ss3644906562, ss3646334850, ss3653112593, ss3653112594, ss3654128248, ss3666711841, ss3733362632, ss3744550015, ss3745357248, ss3764823712, ss3785425927, ss3790785298, ss3795662816, ss3824170770, ss3825694375, ss3829833357, ss3838395031, ss3864256575, ss3911031803, ss3984333351, ss3984565782, ss3985213241, ss5176840346, ss5315142449, ss5364726791, ss5508428939, ss5623935748, ss5624623903, ss5640091137, ss5800055678, ss5800129075, ss5842028327, ss5847291071, ss5848089872, ss5848651544, ss5936530753, ss5968592985, ss5979780294, ss5980356802, ss5981234488	NC_000006.11:31611776:T:C	NC_000006.12:31643999:T:C	(self)
41122496, 221235365, 500714, 48533460, 535787359, 13239536269, ss2282950019, ss3025608573, ss3648310221, ss3716910380, ss3726330387, ss3771279245, ss3807978829, ss3843837220, ss4698409801, ss5237190552, ss5267939296, ss5465672953, ss5553596561, ss5714696356, ss5807308483, ss5855284413, ss5883246748	NC_000006.12:31643999:T:C	NC_000006.12:31643999:T:C	(self)
ss11797655, ss17107920, ss19659647, ss22424818	NT_007592.13:22466328:T:C	NC_000006.12:31643999:T:C	(self)
ss133122, ss3199053, ss4377962, ss12691574, ss23137850, ss65842182, ss71644732, ss81436843, ss98379899, ss105991228, ss139847526, ss156748345, ss160893921	NT_007592.15:31551776:T:C	NC_000006.12:31643999:T:C	(self)
ss4025188829	NT_113891.3:3121288:C:C	NC_000006.12:31643999:T:C	(self)
ss4025209488	NT_167245.2:2891765:C:C	NC_000006.12:31643999:T:C	(self)
ss4025229550	NT_167246.2:2949045:C:C	NC_000006.12:31643999:T:C	(self)
ss4025248191	NT_167247.2:2985864:C:C	NC_000006.12:31643999:T:C	(self)
ss4025266906	NT_167248.2:2899820:C:C	NC_000006.12:31643999:T:C	(self)
18209197, ss3911031803	NC_000006.11:31611776:T:G	NC_000006.12:31643999:T:G	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs760293

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs760293