Name: rs7144302
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.

rs7144302

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:72280815 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.358771 (94963/264690, TOPMED)
C=0.366920 (51385/140044, GnomAD)
C=0.41094 (12094/29430, ALFA) (+ 19 more)
C=0.42791 (12092/28258, 14KJPN)
C=0.42405 (7107/16760, 8.3KJPN)
C=0.3406 (2181/6404, 1000G_30x)
C=0.3482 (1744/5008, 1000G)
C=0.4837 (2167/4480, Estonian)
C=0.4549 (1753/3854, ALSPAC)
C=0.4744 (1759/3708, TWINSUK)
C=0.3437 (1007/2930, KOREAN)
C=0.3148 (595/1890, HapMap)
C=0.3428 (628/1832, Korea1K)
C=0.465 (464/998, GoNL)
C=0.409 (256/626, Chileans)
C=0.425 (255/600, NorthernSweden)
T=0.362 (113/312, SGDP_PRJ)
C=0.319 (69/216, Qatari)
C=0.340 (72/212, Vietnamese)
T=0.48 (20/42, Ancient Sardinia)
T=0.47 (19/40, GENOME_DK)
T=0.31 (10/32, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RGS6 : 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	29430	T=0.58906	C=0.41094
European	Sub	19510	T=0.52758	C=0.47242
African	Sub	4792	T=0.8218	C=0.1782
African Others	Sub	160	T=0.875	C=0.125
African American	Sub	4632	T=0.8199	C=0.1801
Asian	Sub	172	T=0.721	C=0.279
East Asian	Sub	112	T=0.714	C=0.286
Other Asian	Sub	60	T=0.73	C=0.27
Latin American 1	Sub	312	T=0.606	C=0.394
Latin American 2	Sub	2830	T=0.6039	C=0.3961
South Asian	Sub	110	T=0.582	C=0.418
Other	Sub	1704	T=0.5980	C=0.4020

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=0.641229	C=0.358771
gnomAD - Genomes	Global	Study-wide	140044	T=0.633080	C=0.366920
gnomAD - Genomes	European	Sub	75854	T=0.53554	C=0.46446
gnomAD - Genomes	African	Sub	41958	T=0.82244	C=0.17756
gnomAD - Genomes	American	Sub	13638	T=0.60940	C=0.39060
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.5256	C=0.4744
gnomAD - Genomes	East Asian	Sub	3126	T=0.6759	C=0.3241
gnomAD - Genomes	Other	Sub	2144	T=0.6329	C=0.3671
Allele Frequency Aggregator	Total	Global	29430	T=0.58906	C=0.41094
Allele Frequency Aggregator	European	Sub	19510	T=0.52758	C=0.47242
Allele Frequency Aggregator	African	Sub	4792	T=0.8218	C=0.1782
Allele Frequency Aggregator	Latin American 2	Sub	2830	T=0.6039	C=0.3961
Allele Frequency Aggregator	Other	Sub	1704	T=0.5980	C=0.4020
Allele Frequency Aggregator	Latin American 1	Sub	312	T=0.606	C=0.394
Allele Frequency Aggregator	Asian	Sub	172	T=0.721	C=0.279
Allele Frequency Aggregator	South Asian	Sub	110	T=0.582	C=0.418
14KJPN	JAPANESE	Study-wide	28258	T=0.57209	C=0.42791
8.3KJPN	JAPANESE	Study-wide	16760	T=0.57595	C=0.42405
1000Genomes_30x	Global	Study-wide	6404	T=0.6594	C=0.3406
1000Genomes_30x	African	Sub	1786	T=0.8499	C=0.1501
1000Genomes_30x	Europe	Sub	1266	T=0.5348	C=0.4652
1000Genomes_30x	South Asian	Sub	1202	T=0.6364	C=0.3636
1000Genomes_30x	East Asian	Sub	1170	T=0.6060	C=0.3940
1000Genomes_30x	American	Sub	980	T=0.565	C=0.435
1000Genomes	Global	Study-wide	5008	T=0.6518	C=0.3482
1000Genomes	African	Sub	1322	T=0.8502	C=0.1498
1000Genomes	East Asian	Sub	1008	T=0.5982	C=0.4018
1000Genomes	Europe	Sub	1006	T=0.5408	C=0.4592
1000Genomes	South Asian	Sub	978	T=0.622	C=0.378
1000Genomes	American	Sub	694	T=0.555	C=0.445
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.5163	C=0.4837
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.5451	C=0.4549
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.5256	C=0.4744
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.6563	A=0.0000, C=0.3437
HapMap	Global	Study-wide	1890	T=0.6852	C=0.3148
HapMap	American	Sub	770	T=0.596	C=0.404
HapMap	African	Sub	690	T=0.864	C=0.136
HapMap	Asian	Sub	254	T=0.602	C=0.398
HapMap	Europe	Sub	176	T=0.494	C=0.506
Korean Genome Project	KOREAN	Study-wide	1832	T=0.6572	C=0.3428
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.535	C=0.465
Chileans	Chilean	Study-wide	626	T=0.591	C=0.409
Northern Sweden	ACPOP	Study-wide	600	T=0.575	C=0.425
SGDP_PRJ	Global	Study-wide	312	T=0.362	C=0.638
Qatari	Global	Study-wide	216	T=0.681	C=0.319
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.660	C=0.340
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	42	T=0.48	C=0.52
The Danish reference pan genome	Danish	Study-wide	40	T=0.47	C=0.53
Siberian	Global	Study-wide	32	T=0.31	C=0.69

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 14	NC_000014.9:g.72280815T>A
GRCh38.p14 chr 14	NC_000014.9:g.72280815T>C
GRCh37.p13 chr 14	NC_000014.8:g.72747523T>A
GRCh37.p13 chr 14	NC_000014.8:g.72747523T>C
RGS6 RefSeqGene	NG_029236.1:g.353707T>A
RGS6 RefSeqGene	NG_029236.1:g.353707T>C

Gene: RGS6, regulator of G protein signaling 6 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RGS6 transcript variant 1	NM_001204416.3:c.85-71280… NM_001204416.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 3	NM_001204417.3:c.85-71280… NM_001204417.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 4	NM_001204418.3:c.85-71280… NM_001204418.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 5	NM_001204419.3:c.85-71280… NM_001204419.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 6	NM_001204420.3:c.85-71280… NM_001204420.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 7	NM_001204421.3:c.85-71280… NM_001204421.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 8	NM_001204422.3:c.85-71280… NM_001204422.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 9	NM_001204423.2:c.-21-7128… NM_001204423.2:c.-21-71280T>A	N/A	Intron Variant
RGS6 transcript variant 10	NM_001204424.2:c.85-71280… NM_001204424.2:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 12	NM_001370270.1:c.85-71280… NM_001370270.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 13	NM_001370271.1:c.85-71280… NM_001370271.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 14	NM_001370272.1:c.85-71280… NM_001370272.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 15	NM_001370273.1:c.85-71280… NM_001370273.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 16	NM_001370274.1:c.85-71280… NM_001370274.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 17	NM_001370275.1:c.85-71280… NM_001370275.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 18	NM_001370276.1:c.85-71280… NM_001370276.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 19	NM_001370277.1:c.85-71280… NM_001370277.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 20	NM_001370278.1:c.85-71280… NM_001370278.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 21	NM_001370279.1:c.85-71280… NM_001370279.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 22	NM_001370280.1:c.85-71280… NM_001370280.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 23	NM_001370281.1:c.85-71280… NM_001370281.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 24	NM_001370282.1:c.85-71280… NM_001370282.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 25	NM_001370283.1:c.85-71280… NM_001370283.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 26	NM_001370284.1:c.85-71280… NM_001370284.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 27	NM_001370286.1:c.85-71280… NM_001370286.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 28	NM_001370287.1:c.85-71280… NM_001370287.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 29	NM_001370288.1:c.85-71280… NM_001370288.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 30	NM_001370289.1:c.85-71280… NM_001370289.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 31	NM_001370290.1:c.85-71280… NM_001370290.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 32	NM_001370291.1:c.85-71280… NM_001370291.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 33	NM_001370292.1:c.85-71280… NM_001370292.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 34	NM_001370293.1:c.85-71280… NM_001370293.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 35	NM_001370294.1:c.85-71280… NM_001370294.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 2	NM_004296.7:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant 11	NR_135235.2:n.	N/A	Intron Variant
RGS6 transcript variant X4	XM_017021820.3:c.85-71280… XM_017021820.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X9	XM_017021822.3:c.85-71280… XM_017021822.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X11	XM_017021825.3:c.85-71280… XM_017021825.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X12	XM_017021826.3:c.85-71280… XM_017021826.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X13	XM_017021827.3:c.85-71280… XM_017021827.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X15	XM_017021828.3:c.85-71280… XM_017021828.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X16	XM_017021830.3:c.85-71280… XM_017021830.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X17	XM_017021831.3:c.85-71280… XM_017021831.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X18	XM_017021832.3:c.85-71280… XM_017021832.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X21	XM_017021833.3:c.85-71280… XM_017021833.3:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X1	XM_024449759.2:c.85-71280… XM_024449759.2:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X3	XM_024449760.2:c.85-71280… XM_024449760.2:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X2	XM_024449761.2:c.85-71280… XM_024449761.2:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X19	XM_024449776.2:c.85-71280… XM_024449776.2:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X10	XM_047431987.1:c.85-71280… XM_047431987.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X20	XM_047431990.1:c.85-71280… XM_047431990.1:c.85-71280T>A	N/A	Intron Variant
RGS6 transcript variant X8	XM_011537397.2:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X6	XM_024449763.2:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X7	XM_024449764.2:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X5	XM_047431985.1:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X14	XM_047431988.1:c.	N/A	Genic Upstream Transcript 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
GRCh38.p14 chr 14	NC_000014.9:g.72280815=	NC_000014.9:g.72280815T>A	NC_000014.9:g.72280815T>C
GRCh37.p13 chr 14	NC_000014.8:g.72747523=	NC_000014.8:g.72747523T>A	NC_000014.8:g.72747523T>C
RGS6 RefSeqGene	NG_029236.1:g.353707=	NG_029236.1:g.353707T>A	NG_029236.1:g.353707T>C
RGS6 transcript variant 1	NM_001204416.1:c.85-71280=	NM_001204416.1:c.85-71280T>A	NM_001204416.1:c.85-71280T>C
RGS6 transcript variant 1	NM_001204416.3:c.85-71280=	NM_001204416.3:c.85-71280T>A	NM_001204416.3:c.85-71280T>C
RGS6 transcript variant 3	NM_001204417.1:c.85-71280=	NM_001204417.1:c.85-71280T>A	NM_001204417.1:c.85-71280T>C
RGS6 transcript variant 3	NM_001204417.3:c.85-71280=	NM_001204417.3:c.85-71280T>A	NM_001204417.3:c.85-71280T>C
RGS6 transcript variant 4	NM_001204418.1:c.85-71280=	NM_001204418.1:c.85-71280T>A	NM_001204418.1:c.85-71280T>C
RGS6 transcript variant 4	NM_001204418.3:c.85-71280=	NM_001204418.3:c.85-71280T>A	NM_001204418.3:c.85-71280T>C
RGS6 transcript variant 5	NM_001204419.1:c.85-71280=	NM_001204419.1:c.85-71280T>A	NM_001204419.1:c.85-71280T>C
RGS6 transcript variant 5	NM_001204419.3:c.85-71280=	NM_001204419.3:c.85-71280T>A	NM_001204419.3:c.85-71280T>C
RGS6 transcript variant 6	NM_001204420.1:c.85-71280=	NM_001204420.1:c.85-71280T>A	NM_001204420.1:c.85-71280T>C
RGS6 transcript variant 6	NM_001204420.3:c.85-71280=	NM_001204420.3:c.85-71280T>A	NM_001204420.3:c.85-71280T>C
RGS6 transcript variant 7	NM_001204421.1:c.85-71280=	NM_001204421.1:c.85-71280T>A	NM_001204421.1:c.85-71280T>C
RGS6 transcript variant 7	NM_001204421.3:c.85-71280=	NM_001204421.3:c.85-71280T>A	NM_001204421.3:c.85-71280T>C
RGS6 transcript variant 8	NM_001204422.1:c.85-71280=	NM_001204422.1:c.85-71280T>A	NM_001204422.1:c.85-71280T>C
RGS6 transcript variant 8	NM_001204422.3:c.85-71280=	NM_001204422.3:c.85-71280T>A	NM_001204422.3:c.85-71280T>C
RGS6 transcript variant 9	NM_001204423.1:c.-21-71280=	NM_001204423.1:c.-21-71280T>A	NM_001204423.1:c.-21-71280T>C
RGS6 transcript variant 9	NM_001204423.2:c.-21-71280=	NM_001204423.2:c.-21-71280T>A	NM_001204423.2:c.-21-71280T>C
RGS6 transcript variant 10	NM_001204424.1:c.85-71280=	NM_001204424.1:c.85-71280T>A	NM_001204424.1:c.85-71280T>C
RGS6 transcript variant 10	NM_001204424.2:c.85-71280=	NM_001204424.2:c.85-71280T>A	NM_001204424.2:c.85-71280T>C
RGS6 transcript variant 12	NM_001370270.1:c.85-71280=	NM_001370270.1:c.85-71280T>A	NM_001370270.1:c.85-71280T>C
RGS6 transcript variant 13	NM_001370271.1:c.85-71280=	NM_001370271.1:c.85-71280T>A	NM_001370271.1:c.85-71280T>C
RGS6 transcript variant 14	NM_001370272.1:c.85-71280=	NM_001370272.1:c.85-71280T>A	NM_001370272.1:c.85-71280T>C
RGS6 transcript variant 15	NM_001370273.1:c.85-71280=	NM_001370273.1:c.85-71280T>A	NM_001370273.1:c.85-71280T>C
RGS6 transcript variant 16	NM_001370274.1:c.85-71280=	NM_001370274.1:c.85-71280T>A	NM_001370274.1:c.85-71280T>C
RGS6 transcript variant 17	NM_001370275.1:c.85-71280=	NM_001370275.1:c.85-71280T>A	NM_001370275.1:c.85-71280T>C
RGS6 transcript variant 18	NM_001370276.1:c.85-71280=	NM_001370276.1:c.85-71280T>A	NM_001370276.1:c.85-71280T>C
RGS6 transcript variant 19	NM_001370277.1:c.85-71280=	NM_001370277.1:c.85-71280T>A	NM_001370277.1:c.85-71280T>C
RGS6 transcript variant 20	NM_001370278.1:c.85-71280=	NM_001370278.1:c.85-71280T>A	NM_001370278.1:c.85-71280T>C
RGS6 transcript variant 21	NM_001370279.1:c.85-71280=	NM_001370279.1:c.85-71280T>A	NM_001370279.1:c.85-71280T>C
RGS6 transcript variant 22	NM_001370280.1:c.85-71280=	NM_001370280.1:c.85-71280T>A	NM_001370280.1:c.85-71280T>C
RGS6 transcript variant 23	NM_001370281.1:c.85-71280=	NM_001370281.1:c.85-71280T>A	NM_001370281.1:c.85-71280T>C
RGS6 transcript variant 24	NM_001370282.1:c.85-71280=	NM_001370282.1:c.85-71280T>A	NM_001370282.1:c.85-71280T>C
RGS6 transcript variant 25	NM_001370283.1:c.85-71280=	NM_001370283.1:c.85-71280T>A	NM_001370283.1:c.85-71280T>C
RGS6 transcript variant 26	NM_001370284.1:c.85-71280=	NM_001370284.1:c.85-71280T>A	NM_001370284.1:c.85-71280T>C
RGS6 transcript variant 27	NM_001370286.1:c.85-71280=	NM_001370286.1:c.85-71280T>A	NM_001370286.1:c.85-71280T>C
RGS6 transcript variant 28	NM_001370287.1:c.85-71280=	NM_001370287.1:c.85-71280T>A	NM_001370287.1:c.85-71280T>C
RGS6 transcript variant 29	NM_001370288.1:c.85-71280=	NM_001370288.1:c.85-71280T>A	NM_001370288.1:c.85-71280T>C
RGS6 transcript variant 30	NM_001370289.1:c.85-71280=	NM_001370289.1:c.85-71280T>A	NM_001370289.1:c.85-71280T>C
RGS6 transcript variant 31	NM_001370290.1:c.85-71280=	NM_001370290.1:c.85-71280T>A	NM_001370290.1:c.85-71280T>C
RGS6 transcript variant 32	NM_001370291.1:c.85-71280=	NM_001370291.1:c.85-71280T>A	NM_001370291.1:c.85-71280T>C
RGS6 transcript variant 33	NM_001370292.1:c.85-71280=	NM_001370292.1:c.85-71280T>A	NM_001370292.1:c.85-71280T>C
RGS6 transcript variant 34	NM_001370293.1:c.85-71280=	NM_001370293.1:c.85-71280T>A	NM_001370293.1:c.85-71280T>C
RGS6 transcript variant 35	NM_001370294.1:c.85-71280=	NM_001370294.1:c.85-71280T>A	NM_001370294.1:c.85-71280T>C
RGS6 transcript variant 2	NM_004296.5:c.85-71280=	NM_004296.5:c.85-71280T>A	NM_004296.5:c.85-71280T>C
RGS6 transcript variant 2	NM_004296.7:c.85-71280=	NM_004296.7:c.85-71280T>A	NM_004296.7:c.85-71280T>C
RGS6 transcript variant X1	XM_005268231.1:c.85-71280=	XM_005268231.1:c.85-71280T>A	XM_005268231.1:c.85-71280T>C
RGS6 transcript variant X3	XM_005268233.1:c.85-71280=	XM_005268233.1:c.85-71280T>A	XM_005268233.1:c.85-71280T>C
RGS6 transcript variant X4	XM_005268234.1:c.85-71280=	XM_005268234.1:c.85-71280T>A	XM_005268234.1:c.85-71280T>C
RGS6 transcript variant X5	XM_005268235.1:c.85-71280=	XM_005268235.1:c.85-71280T>A	XM_005268235.1:c.85-71280T>C
RGS6 transcript variant X21	XM_005268236.1:c.85-71280=	XM_005268236.1:c.85-71280T>A	XM_005268236.1:c.85-71280T>C
RGS6 transcript variant X4	XM_017021820.3:c.85-71280=	XM_017021820.3:c.85-71280T>A	XM_017021820.3:c.85-71280T>C
RGS6 transcript variant X9	XM_017021822.3:c.85-71280=	XM_017021822.3:c.85-71280T>A	XM_017021822.3:c.85-71280T>C
RGS6 transcript variant X11	XM_017021825.3:c.85-71280=	XM_017021825.3:c.85-71280T>A	XM_017021825.3:c.85-71280T>C
RGS6 transcript variant X12	XM_017021826.3:c.85-71280=	XM_017021826.3:c.85-71280T>A	XM_017021826.3:c.85-71280T>C
RGS6 transcript variant X13	XM_017021827.3:c.85-71280=	XM_017021827.3:c.85-71280T>A	XM_017021827.3:c.85-71280T>C
RGS6 transcript variant X15	XM_017021828.3:c.85-71280=	XM_017021828.3:c.85-71280T>A	XM_017021828.3:c.85-71280T>C
RGS6 transcript variant X16	XM_017021830.3:c.85-71280=	XM_017021830.3:c.85-71280T>A	XM_017021830.3:c.85-71280T>C
RGS6 transcript variant X17	XM_017021831.3:c.85-71280=	XM_017021831.3:c.85-71280T>A	XM_017021831.3:c.85-71280T>C
RGS6 transcript variant X18	XM_017021832.3:c.85-71280=	XM_017021832.3:c.85-71280T>A	XM_017021832.3:c.85-71280T>C
RGS6 transcript variant X21	XM_017021833.3:c.85-71280=	XM_017021833.3:c.85-71280T>A	XM_017021833.3:c.85-71280T>C
RGS6 transcript variant X1	XM_024449759.2:c.85-71280=	XM_024449759.2:c.85-71280T>A	XM_024449759.2:c.85-71280T>C
RGS6 transcript variant X3	XM_024449760.2:c.85-71280=	XM_024449760.2:c.85-71280T>A	XM_024449760.2:c.85-71280T>C
RGS6 transcript variant X2	XM_024449761.2:c.85-71280=	XM_024449761.2:c.85-71280T>A	XM_024449761.2:c.85-71280T>C
RGS6 transcript variant X19	XM_024449776.2:c.85-71280=	XM_024449776.2:c.85-71280T>A	XM_024449776.2:c.85-71280T>C
RGS6 transcript variant X10	XM_047431987.1:c.85-71280=	XM_047431987.1:c.85-71280T>A	XM_047431987.1:c.85-71280T>C
RGS6 transcript variant X20	XM_047431990.1:c.85-71280=	XM_047431990.1:c.85-71280T>A	XM_047431990.1:c.85-71280T>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#.

80 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10729533	Jul 11, 2003 (116)
2	PERLEGEN	ss24605915	Sep 20, 2004 (123)
3	ABI	ss43623287	Mar 15, 2006 (126)
4	ILLUMINA	ss75168250	Dec 07, 2007 (129)
5	AFFY	ss76464132	Dec 08, 2007 (130)
6	BCMHGSC_JDW	ss89990594	Mar 24, 2008 (129)
7	HUMANGENOME_JCVI	ss96927318	Feb 04, 2009 (130)
8	BGI	ss103197788	Feb 04, 2009 (130)
9	KRIBB_YJKIM	ss119543203	Dec 01, 2009 (131)
10	ENSEMBL	ss134042867	Dec 01, 2009 (131)
11	ENSEMBL	ss142661030	Dec 01, 2009 (131)
12	COMPLETE_GENOMICS	ss171304347	Jul 04, 2010 (132)
13	ILLUMINA	ss174260117	Jul 04, 2010 (132)
14	BUSHMAN	ss200246966	Jul 04, 2010 (132)
15	BCM-HGSC-SUB	ss206954028	Jul 04, 2010 (132)
16	1000GENOMES	ss226642853	Jul 14, 2010 (132)
17	1000GENOMES	ss236597706	Jul 15, 2010 (132)
18	1000GENOMES	ss243019984	Jul 15, 2010 (132)
19	BL	ss255093261	May 09, 2011 (134)
20	GMI	ss282057911	May 04, 2012 (137)
21	GMI	ss286866781	Apr 25, 2013 (138)
22	PJP	ss291626848	May 09, 2011 (134)
23	ILLUMINA	ss537440674	Sep 08, 2015 (146)
24	TISHKOFF	ss564178329	Apr 25, 2013 (138)
25	SSMP	ss659868198	Apr 25, 2013 (138)
26	EVA-GONL	ss991298267	Aug 21, 2014 (142)
27	JMKIDD_LAB	ss1079767498	Aug 21, 2014 (142)
28	1000GENOMES	ss1351575220	Aug 21, 2014 (142)
29	DDI	ss1427466199	Apr 01, 2015 (144)
30	EVA_GENOME_DK	ss1577343010	Apr 01, 2015 (144)
31	EVA_UK10K_ALSPAC	ss1632044681	Apr 01, 2015 (144)
32	EVA_UK10K_TWINSUK	ss1675038714	Apr 01, 2015 (144)
33	EVA_DECODE	ss1695302278	Apr 01, 2015 (144)
34	EVA_SVP	ss1713455429	Apr 01, 2015 (144)
35	WEILL_CORNELL_DGM	ss1934668878	Feb 12, 2016 (147)
36	GENOMED	ss1967994975	Jul 19, 2016 (147)
37	JJLAB	ss2028116578	Sep 14, 2016 (149)
38	USC_VALOUEV	ss2156491627	Dec 20, 2016 (150)
39	HUMAN_LONGEVITY	ss2203168496	Dec 20, 2016 (150)
40	SYSTEMSBIOZJU	ss2628546837	Nov 08, 2017 (151)
41	ILLUMINA	ss2633169304	Nov 08, 2017 (151)
42	GRF	ss2700923438	Nov 08, 2017 (151)
43	GNOMAD	ss2929324591	Nov 08, 2017 (151)
44	SWEGEN	ss3012434660	Nov 08, 2017 (151)
45	BIOINF_KMB_FNS_UNIBA	ss3027882752	Nov 08, 2017 (151)
46	CSHL	ss3350873328	Nov 08, 2017 (151)
47	ILLUMINA	ss3627252296	Oct 12, 2018 (152)
48	ILLUMINA	ss3638058752	Oct 12, 2018 (152)
49	ILLUMINA	ss3643044940	Oct 12, 2018 (152)
50	URBANLAB	ss3650235286	Oct 12, 2018 (152)
51	EGCUT_WGS	ss3679691574	Jul 13, 2019 (153)
52	EVA_DECODE	ss3696961295	Jul 13, 2019 (153)
53	ACPOP	ss3740508820	Jul 13, 2019 (153)
54	EVA	ss3752498619	Jul 13, 2019 (153)
55	PACBIO	ss3787704878	Jul 13, 2019 (153)
56	PACBIO	ss3792736781	Jul 13, 2019 (153)
57	PACBIO	ss3797621116	Jul 13, 2019 (153)
58	KHV_HUMAN_GENOMES	ss3817825971	Jul 13, 2019 (153)
59	EVA	ss3833993036	Apr 27, 2020 (154)
60	EVA	ss3840587929	Apr 27, 2020 (154)
61	EVA	ss3846077459	Apr 27, 2020 (154)
62	SGDP_PRJ	ss3881805339	Apr 27, 2020 (154)
63	KRGDB	ss3930853547	Apr 27, 2020 (154)
64	KOGIC	ss3975213303	Apr 27, 2020 (154)
65	EVA	ss3985688425	Apr 27, 2021 (155)
66	EVA	ss4017677793	Apr 27, 2021 (155)
67	TOPMED	ss4975618683	Apr 27, 2021 (155)
68	TOMMO_GENOMICS	ss5213877259	Apr 27, 2021 (155)
69	1000G_HIGH_COVERAGE	ss5296723360	Oct 17, 2022 (156)
70	EVA	ss5416170218	Oct 17, 2022 (156)
71	HUGCELL_USP	ss5490718281	Oct 17, 2022 (156)
72	EVA	ss5511293621	Oct 17, 2022 (156)
73	1000G_HIGH_COVERAGE	ss5597255833	Oct 17, 2022 (156)
74	SANFORD_IMAGENETICS	ss5656504205	Oct 17, 2022 (156)
75	TOMMO_GENOMICS	ss5766866509	Oct 17, 2022 (156)
76	YY_MCH	ss5814875111	Oct 17, 2022 (156)
77	EVA	ss5841307248	Oct 17, 2022 (156)
78	EVA	ss5851094779	Oct 17, 2022 (156)
79	EVA	ss5901917082	Oct 17, 2022 (156)
80	EVA	ss5947950784	Oct 17, 2022 (156)
81	1000Genomes	NC_000014.8 - 72747523	Oct 12, 2018 (152)
82	1000Genomes_30x	NC_000014.9 - 72280815	Oct 17, 2022 (156)
83	The Avon Longitudinal Study of Parents and Children	NC_000014.8 - 72747523	Oct 12, 2018 (152)
84	Chileans	NC_000014.8 - 72747523	Apr 27, 2020 (154)
85	Genetic variation in the Estonian population	NC_000014.8 - 72747523	Oct 12, 2018 (152)
86	The Danish reference pan genome	NC_000014.8 - 72747523	Apr 27, 2020 (154)
87	gnomAD - Genomes	NC_000014.9 - 72280815	Apr 27, 2021 (155)
88	Genome of the Netherlands Release 5	NC_000014.8 - 72747523	Apr 27, 2020 (154)
89	HapMap	NC_000014.9 - 72280815	Apr 27, 2020 (154)
90	KOREAN population from KRGDB	NC_000014.8 - 72747523	Apr 27, 2020 (154)
91	Korean Genome Project	NC_000014.9 - 72280815	Apr 27, 2020 (154)
92	Northern Sweden	NC_000014.8 - 72747523	Jul 13, 2019 (153)
93	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000014.8 - 72747523	Apr 27, 2021 (155)
94	Qatari	NC_000014.8 - 72747523	Apr 27, 2020 (154)
95	SGDP_PRJ	NC_000014.8 - 72747523	Apr 27, 2020 (154)
96	Siberian	NC_000014.8 - 72747523	Apr 27, 2020 (154)
97	8.3KJPN	NC_000014.8 - 72747523	Apr 27, 2021 (155)
98	14KJPN	NC_000014.9 - 72280815	Oct 17, 2022 (156)
99	TopMed	NC_000014.9 - 72280815	Apr 27, 2021 (155)
100	UK 10K study - Twins	NC_000014.8 - 72747523	Oct 12, 2018 (152)
101	A Vietnamese Genetic Variation Database	NC_000014.8 - 72747523	Jul 13, 2019 (153)
102	ALFA	NC_000014.9 - 72280815	Apr 27, 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)
rs17180335	Oct 08, 2004 (123)
rs56428802	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
38030941, ss3930853547	NC_000014.8:72747522:T:A	NC_000014.9:72280814:T:A	(self)
ss76464132, ss89990594, ss171304347, ss200246966, ss206954028, ss255093261, ss282057911, ss286866781, ss291626848, ss1695302278, ss1713455429, ss3643044940	NC_000014.7:71817275:T:C	NC_000014.9:72280814:T:C	(self)
64577598, 35884308, 141541, 25429822, 3662837, 16025389, 38030941, 13793685, 914352, 16710808, 33822319, 9007981, 71846566, 35884308, 7982087, ss226642853, ss236597706, ss243019984, ss537440674, ss564178329, ss659868198, ss991298267, ss1079767498, ss1351575220, ss1427466199, ss1577343010, ss1632044681, ss1675038714, ss1934668878, ss1967994975, ss2028116578, ss2156491627, ss2628546837, ss2633169304, ss2700923438, ss2929324591, ss3012434660, ss3350873328, ss3627252296, ss3638058752, ss3679691574, ss3740508820, ss3752498619, ss3787704878, ss3792736781, ss3797621116, ss3833993036, ss3840587929, ss3881805339, ss3930853547, ss3985688425, ss4017677793, ss5213877259, ss5416170218, ss5511293621, ss5656504205, ss5841307248, ss5947950784	NC_000014.8:72747522:T:C	NC_000014.9:72280814:T:C	(self)
84781768, 455322019, 1173179, 31591304, 100703613, 191164342, 8416014363, ss2203168496, ss3027882752, ss3650235286, ss3696961295, ss3817825971, ss3846077459, ss3975213303, ss4975618683, ss5296723360, ss5490718281, ss5597255833, ss5766866509, ss5814875111, ss5851094779, ss5901917082	NC_000014.9:72280814:T:C	NC_000014.9:72280814:T:C	(self)
ss10729533	NT_026437.10:52667563:T:C	NC_000014.9:72280814:T:C	(self)
ss24605915, ss43623287, ss75168250, ss96927318, ss103197788, ss119543203, ss134042867, ss142661030, ss174260117	NT_026437.12:53747522:T:C	NC_000014.9:72280814:T:C	(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 rs7144302

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs7144302