Name: rs6850727
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.

rs6850727

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:1329485 (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: G>A / G>C / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.333299 (88221/264690, TOPMED)
C=0.39921 (11281/28258, 14KJPN)
C=0.40149 (6729/16760, 8.3KJPN) (+ 16 more)
C=0.07571 (1029/13592, ALFA)
C=0.4007 (2566/6404, 1000G_30x)
C=0.3926 (1966/5008, 1000G)
C=0.1250 (560/4480, Estonian)
C=0.1658 (639/3854, ALSPAC)
C=0.1561 (579/3708, TWINSUK)
C=0.4355 (1275/2928, KOREAN)
C=0.4230 (775/1832, Korea1K)
C=0.151 (151/998, GoNL)
C=0.165 (99/600, NorthernSweden)
G=0.336 (109/324, SGDP_PRJ)
C=0.241 (52/216, Qatari)
G=0.500 (105/210, Vietnamese)
C=0.500 (105/210, Vietnamese)
C=0.17 (7/40, GENOME_DK)
G=0.33 (6/18, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MAEA : 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	13592	G=0.92429	A=0.00000, C=0.07571, T=0.00000
European	Sub	12162	G=0.92526	A=0.00000, C=0.07474, T=0.00000
African	Sub	624	G=0.888	A=0.000, C=0.112, T=0.000
African Others	Sub	18	G=0.94	A=0.00, C=0.06, T=0.00
African American	Sub	606	G=0.886	A=0.000, C=0.114, T=0.000
Asian	Sub	32	G=0.94	A=0.00, C=0.06, T=0.00
East Asian	Sub	22	G=0.91	A=0.00, C=0.09, T=0.00
Other Asian	Sub	10	G=1.0	A=0.0, C=0.0, T=0.0
Latin American 1	Sub	78	G=1.00	A=0.00, C=0.00, T=0.00
Latin American 2	Sub	212	G=1.000	A=0.000, C=0.000, T=0.000
South Asian	Sub	70	G=0.99	A=0.00, C=0.01, T=0.00
Other	Sub	414	G=0.886	A=0.000, C=0.114, T=0.000

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	G=0.666701	C=0.333299
14KJPN	JAPANESE	Study-wide	28258	G=0.60079	C=0.39921
8.3KJPN	JAPANESE	Study-wide	16760	G=0.59851	C=0.40149
Allele Frequency Aggregator	Total	Global	13592	G=0.92429	A=0.00000, C=0.07571, T=0.00000
Allele Frequency Aggregator	European	Sub	12162	G=0.92526	A=0.00000, C=0.07474, T=0.00000
Allele Frequency Aggregator	African	Sub	624	G=0.888	A=0.000, C=0.112, T=0.000
Allele Frequency Aggregator	Other	Sub	414	G=0.886	A=0.000, C=0.114, T=0.000
Allele Frequency Aggregator	Latin American 2	Sub	212	G=1.000	A=0.000, C=0.000, T=0.000
Allele Frequency Aggregator	Latin American 1	Sub	78	G=1.00	A=0.00, C=0.00, T=0.00
Allele Frequency Aggregator	South Asian	Sub	70	G=0.99	A=0.00, C=0.01, T=0.00
Allele Frequency Aggregator	Asian	Sub	32	G=0.94	A=0.00, C=0.06, T=0.00
1000Genomes_30x	Global	Study-wide	6404	G=0.5993	C=0.4007
1000Genomes_30x	African	Sub	1786	G=0.3561	C=0.6439
1000Genomes_30x	Europe	Sub	1266	G=0.8325	C=0.1675
1000Genomes_30x	South Asian	Sub	1202	G=0.7696	C=0.2304
1000Genomes_30x	East Asian	Sub	1170	G=0.5368	C=0.4632
1000Genomes_30x	American	Sub	980	G=0.607	C=0.393
1000Genomes	Global	Study-wide	5008	G=0.6074	C=0.3926
1000Genomes	African	Sub	1322	G=0.3593	C=0.6407
1000Genomes	East Asian	Sub	1008	G=0.5427	C=0.4573
1000Genomes	Europe	Sub	1006	G=0.8380	C=0.1620
1000Genomes	South Asian	Sub	978	G=0.770	C=0.230
1000Genomes	American	Sub	694	G=0.611	C=0.389
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.8750	C=0.1250
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.8342	C=0.1658
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.8439	C=0.1561
KOREAN population from KRGDB	KOREAN	Study-wide	2928	G=0.5645	C=0.4355
Korean Genome Project	KOREAN	Study-wide	1832	G=0.5770	C=0.4230
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.849	C=0.151
Northern Sweden	ACPOP	Study-wide	600	G=0.835	C=0.165
SGDP_PRJ	Global	Study-wide	324	G=0.336	C=0.664
Qatari	Global	Study-wide	216	G=0.759	C=0.241
A Vietnamese Genetic Variation Database	Global	Study-wide	210	G=0.500	C=0.500
The Danish reference pan genome	Danish	Study-wide	40	G=0.82	C=0.17
Siberian	Global	Study-wide	18	G=0.33	C=0.67

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 4	NC_000004.12:g.1329485G>A
GRCh38.p14 chr 4	NC_000004.12:g.1329485G>C
GRCh38.p14 chr 4	NC_000004.12:g.1329485G>T
GRCh37.p13 chr 4	NC_000004.11:g.1323273G>A
GRCh37.p13 chr 4	NC_000004.11:g.1323273G>C
GRCh37.p13 chr 4	NC_000004.11:g.1323273G>T

Gene: MAEA, macrophage erythroblast attacher, E3 ubiquitin ligase (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAEA transcript variant 1	NM_001017405.3:c.656+1782… NM_001017405.3:c.656+1782G>A	N/A	Intron Variant
MAEA transcript variant 3	NM_001297430.2:c.452+1782… NM_001297430.2:c.452+1782G>A	N/A	Intron Variant
MAEA transcript variant 4	NM_001297431.2:c.457-3272… NM_001297431.2:c.457-3272G>A	N/A	Intron Variant
MAEA transcript variant 5	NM_001297432.2:c.653+1782… NM_001297432.2:c.653+1782G>A	N/A	Intron Variant
MAEA transcript variant 6	NM_001297433.2:c.512+1782… NM_001297433.2:c.512+1782G>A	N/A	Intron Variant
MAEA transcript variant 2	NM_005882.5:c.533+1782G>A	N/A	Intron Variant
MAEA transcript variant 7	NR_123716.2:n.	N/A	Intron Variant
MAEA transcript variant X1	XM_006713849.3:c.656+1782… XM_006713849.3:c.656+1782G>A	N/A	Intron Variant
MAEA transcript variant X2	XM_006713850.3:c.653+1782… XM_006713850.3:c.653+1782G>A	N/A	Intron Variant
MAEA transcript variant X3	XM_047449493.1:c.512+1782… XM_047449493.1:c.512+1782G>A	N/A	Intron Variant
MAEA transcript variant X4	XM_047449494.1:c.580-3272… XM_047449494.1:c.580-3272G>A	N/A	Intron Variant
MAEA transcript variant X5	XM_047449495.1:c.*782=	N/A	3 Prime UTR 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	G=	A	C	T
GRCh38.p14 chr 4	NC_000004.12:g.1329485=	NC_000004.12:g.1329485G>A	NC_000004.12:g.1329485G>C	NC_000004.12:g.1329485G>T
GRCh37.p13 chr 4	NC_000004.11:g.1323273=	NC_000004.11:g.1323273G>A	NC_000004.11:g.1323273G>C	NC_000004.11:g.1323273G>T
MAEA transcript variant X5	XM_047449495.1:c.*782=	XM_047449495.1:c.*782G>A	XM_047449495.1:c.*782G>C	XM_047449495.1:c.*782G>T
MAEA transcript variant 1	NM_001017405.1:c.656+1782=	NM_001017405.1:c.656+1782G>A	NM_001017405.1:c.656+1782G>C	NM_001017405.1:c.656+1782G>T
MAEA transcript variant 1	NM_001017405.3:c.656+1782=	NM_001017405.3:c.656+1782G>A	NM_001017405.3:c.656+1782G>C	NM_001017405.3:c.656+1782G>T
MAEA transcript variant 3	NM_001297430.2:c.452+1782=	NM_001297430.2:c.452+1782G>A	NM_001297430.2:c.452+1782G>C	NM_001297430.2:c.452+1782G>T
MAEA transcript variant 4	NM_001297431.2:c.457-3272=	NM_001297431.2:c.457-3272G>A	NM_001297431.2:c.457-3272G>C	NM_001297431.2:c.457-3272G>T
MAEA transcript variant 5	NM_001297432.2:c.653+1782=	NM_001297432.2:c.653+1782G>A	NM_001297432.2:c.653+1782G>C	NM_001297432.2:c.653+1782G>T
MAEA transcript variant 6	NM_001297433.2:c.512+1782=	NM_001297433.2:c.512+1782G>A	NM_001297433.2:c.512+1782G>C	NM_001297433.2:c.512+1782G>T
MAEA transcript variant 2	NM_005882.3:c.533+1782=	NM_005882.3:c.533+1782G>A	NM_005882.3:c.533+1782G>C	NM_005882.3:c.533+1782G>T
MAEA transcript variant 2	NM_005882.5:c.533+1782=	NM_005882.5:c.533+1782G>A	NM_005882.5:c.533+1782G>C	NM_005882.5:c.533+1782G>T
MAEA transcript variant X1	XM_005272243.1:c.653+1782=	XM_005272243.1:c.653+1782G>A	XM_005272243.1:c.653+1782G>C	XM_005272243.1:c.653+1782G>T
MAEA transcript variant X2	XM_005272244.1:c.512+1782=	XM_005272244.1:c.512+1782G>A	XM_005272244.1:c.512+1782G>C	XM_005272244.1:c.512+1782G>T
MAEA transcript variant X3	XM_005272245.1:c.452+1782=	XM_005272245.1:c.452+1782G>A	XM_005272245.1:c.452+1782G>C	XM_005272245.1:c.452+1782G>T
MAEA transcript variant X4	XM_005272246.1:c.457-3272=	XM_005272246.1:c.457-3272G>A	XM_005272246.1:c.457-3272G>C	XM_005272246.1:c.457-3272G>T
MAEA transcript variant X5	XM_005272247.1:c.656+1782=	XM_005272247.1:c.656+1782G>A	XM_005272247.1:c.656+1782G>C	XM_005272247.1:c.656+1782G>T
MAEA transcript variant X6	XM_005272248.1:c.457-3272=	XM_005272248.1:c.457-3272G>A	XM_005272248.1:c.457-3272G>C	XM_005272248.1:c.457-3272G>T
MAEA transcript variant X1	XM_006713849.3:c.656+1782=	XM_006713849.3:c.656+1782G>A	XM_006713849.3:c.656+1782G>C	XM_006713849.3:c.656+1782G>T
MAEA transcript variant X2	XM_006713850.3:c.653+1782=	XM_006713850.3:c.653+1782G>A	XM_006713850.3:c.653+1782G>C	XM_006713850.3:c.653+1782G>T
MAEA transcript variant X3	XM_047449493.1:c.512+1782=	XM_047449493.1:c.512+1782G>A	XM_047449493.1:c.512+1782G>C	XM_047449493.1:c.512+1782G>T
MAEA transcript variant X4	XM_047449494.1:c.580-3272=	XM_047449494.1:c.580-3272G>A	XM_047449494.1:c.580-3272G>C	XM_047449494.1:c.580-3272G>T

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#.

63 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10174259	Jul 11, 2003 (116)
2	CSHL-HAPMAP	ss17015596	Feb 27, 2004 (120)
3	ABI	ss44477891	Mar 13, 2006 (126)
4	HGSV	ss78854044	Dec 06, 2007 (129)
5	BCMHGSC_JDW	ss92438429	Mar 24, 2008 (129)
6	BGI	ss104032128	Dec 01, 2009 (131)
7	1000GENOMES	ss111654269	Jan 25, 2009 (130)
8	ILLUMINA-UK	ss116836602	Feb 14, 2009 (130)
9	ENSEMBL	ss139393559	Dec 01, 2009 (131)
10	GMI	ss156743315	Dec 01, 2009 (131)
11	COMPLETE_GENOMICS	ss161888128	Jul 04, 2010 (132)
12	COMPLETE_GENOMICS	ss162993451	Jul 04, 2010 (132)
13	1000GENOMES	ss220692178	Jul 14, 2010 (132)
14	1000GENOMES	ss232224249	Jul 14, 2010 (132)
15	1000GENOMES	ss239553516	Jul 15, 2010 (132)
16	GMI	ss277538552	May 04, 2012 (137)
17	PJP	ss293053428	May 09, 2011 (134)
18	TISHKOFF	ss557252265	Apr 25, 2013 (138)
19	SSMP	ss651005628	Apr 25, 2013 (138)
20	EVA-GONL	ss979670427	Aug 21, 2014 (142)
21	JMKIDD_LAB	ss1071213533	Aug 21, 2014 (142)
22	1000GENOMES	ss1308077805	Aug 21, 2014 (142)
23	DDI	ss1429739042	Apr 01, 2015 (144)
24	EVA_GENOME_DK	ss1580379394	Apr 01, 2015 (144)
25	EVA_DECODE	ss1589166800	Apr 01, 2015 (144)
26	EVA_UK10K_ALSPAC	ss1609231188	Apr 01, 2015 (144)
27	EVA_UK10K_TWINSUK	ss1652225221	Apr 01, 2015 (144)
28	HAMMER_LAB	ss1800790001	Sep 08, 2015 (146)
29	WEILL_CORNELL_DGM	ss1922901083	Feb 12, 2016 (147)
30	GENOMED	ss1969636999	Jul 19, 2016 (147)
31	JJLAB	ss2022024360	Sep 14, 2016 (149)
32	USC_VALOUEV	ss2150130297	Dec 20, 2016 (150)
33	HUMAN_LONGEVITY	ss2259801776	Dec 20, 2016 (150)
34	SYSTEMSBIOZJU	ss2625513262	Nov 08, 2017 (151)
35	GRF	ss2705564714	Nov 08, 2017 (151)
36	GNOMAD	ss2804657611	Nov 08, 2017 (151)
37	SWEGEN	ss2993988300	Nov 08, 2017 (151)
38	BIOINF_KMB_FNS_UNIBA	ss3024781790	Nov 08, 2017 (151)
39	CSHL	ss3345497208	Nov 08, 2017 (151)
40	EGCUT_WGS	ss3661926567	Jul 13, 2019 (153)
41	EVA_DECODE	ss3711230963	Jul 13, 2019 (153)
42	EVA_DECODE	ss3711230964	Jul 13, 2019 (153)
43	ACPOP	ss3730775906	Jul 13, 2019 (153)
44	EVA	ss3761281533	Jul 13, 2019 (153)
45	KHV_HUMAN_GENOMES	ss3804421257	Jul 13, 2019 (153)
46	EVA	ss3828324790	Apr 25, 2020 (154)
47	SGDP_PRJ	ss3858017271	Apr 25, 2020 (154)
48	KRGDB	ss3904143768	Apr 25, 2020 (154)
49	KOGIC	ss3953347435	Apr 25, 2020 (154)
50	TOPMED	ss4600084724	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5163805258	Apr 26, 2021 (155)
52	1000G_HIGH_COVERAGE	ss5257732675	Oct 13, 2022 (156)
53	EVA	ss5346355072	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5456687984	Oct 13, 2022 (156)
55	EVA	ss5507367879	Oct 13, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5538026459	Oct 13, 2022 (156)
57	SANFORD_IMAGENETICS	ss5634168300	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5697336189	Oct 13, 2022 (156)
59	YY_MCH	ss5804675206	Oct 13, 2022 (156)
60	EVA	ss5843424948	Oct 13, 2022 (156)
61	EVA	ss5854045339	Oct 13, 2022 (156)
62	EVA	ss5861805340	Oct 13, 2022 (156)
63	EVA	ss5962543816	Oct 13, 2022 (156)
64	1000Genomes	NC_000004.11 - 1323273	Oct 12, 2018 (152)
65	1000Genomes_30x	NC_000004.12 - 1329485	Oct 13, 2022 (156)
66	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 1323273	Oct 12, 2018 (152)
67	Genetic variation in the Estonian population	NC_000004.11 - 1323273	Oct 12, 2018 (152)
68	The Danish reference pan genome	NC_000004.11 - 1323273	Apr 25, 2020 (154)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137830964 (NC_000004.12:1329484:G:A 7/139952) Row 137830965 (NC_000004.12:1329484:G:C 42919/139896) Row 137830966 (NC_000004.12:1329484:G:T 1/139952)	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137830964 (NC_000004.12:1329484:G:A 7/139952) Row 137830965 (NC_000004.12:1329484:G:C 42919/139896) Row 137830966 (NC_000004.12:1329484:G:T 1/139952)	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137830964 (NC_000004.12:1329484:G:A 7/139952) Row 137830965 (NC_000004.12:1329484:G:C 42919/139896) Row 137830966 (NC_000004.12:1329484:G:T 1/139952)	-	Apr 26, 2021 (155)
72	Genome of the Netherlands Release 5	NC_000004.11 - 1323273	Apr 25, 2020 (154)
73	KOREAN population from KRGDB	NC_000004.11 - 1323273	Apr 25, 2020 (154)
74	Korean Genome Project	NC_000004.12 - 1329485	Apr 25, 2020 (154)
75	Northern Sweden	NC_000004.11 - 1323273	Jul 13, 2019 (153)
76	Qatari	NC_000004.11 - 1323273	Apr 25, 2020 (154)
77	SGDP_PRJ	NC_000004.11 - 1323273	Apr 25, 2020 (154)
78	Siberian	NC_000004.11 - 1323273	Apr 25, 2020 (154)
79	8.3KJPN	NC_000004.11 - 1323273	Apr 26, 2021 (155)
80	14KJPN	NC_000004.12 - 1329485	Oct 13, 2022 (156)
81	TopMed	NC_000004.12 - 1329485	Apr 26, 2021 (155)
82	UK 10K study - Twins	NC_000004.11 - 1323273	Oct 12, 2018 (152)
83	A Vietnamese Genetic Variation Database	NC_000004.11 - 1323273	Jul 13, 2019 (153)
84	ALFA	NC_000004.12 - 1329485	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss2804657611	NC_000004.11:1323272:G:A	NC_000004.12:1329484:G:A	(self)
10028609284, ss3711230963	NC_000004.12:1329484:G:A	NC_000004.12:1329484:G:A	(self)
ss78854044	NC_000004.9:1313102:G:C	NC_000004.12:1329484:G:C	(self)
ss92438429, ss111654269, ss116836602, ss161888128, ss162993451, ss277538552, ss293053428, ss1589166800	NC_000004.10:1313272:G:C	NC_000004.12:1329484:G:C	(self)
19415392, 10822804, 7664815, 6544333, 4757042, 11321162, 4060771, 4943013, 10034251, 2646651, 21774565, 10822804, 2366423, ss220692178, ss232224249, ss239553516, ss557252265, ss651005628, ss979670427, ss1071213533, ss1308077805, ss1429739042, ss1580379394, ss1609231188, ss1652225221, ss1800790001, ss1922901083, ss1969636999, ss2022024360, ss2150130297, ss2625513262, ss2705564714, ss2804657611, ss2993988300, ss3345497208, ss3661926567, ss3730775906, ss3761281533, ss3828324790, ss3858017271, ss3904143768, ss5163805258, ss5346355072, ss5507367879, ss5634168300, ss5843424948, ss5962543816	NC_000004.11:1323272:G:C	NC_000004.12:1329484:G:C	(self)
25552394, 9725436, 31173293, 437462280, 10028609284, ss2259801776, ss3024781790, ss3711230964, ss3804421257, ss3953347435, ss4600084724, ss5257732675, ss5456687984, ss5538026459, ss5697336189, ss5804675206, ss5854045339, ss5861805340	NC_000004.12:1329484:G:C	NC_000004.12:1329484:G:C	(self)
ss10174259, ss17015596	NT_037622.3:1313102:G:C	NC_000004.12:1329484:G:C	(self)
ss44477891, ss104032128, ss139393559, ss156743315	NT_037622.5:1313272:G:C	NC_000004.12:1329484:G:C	(self)
10028609284	NC_000004.12:1329484:G:T	NC_000004.12:1329484:G:T	(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 rs6850727

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
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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

rs6850727