Name: rs4660016
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.

rs4660016

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:240972145 (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: A>C / A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.428516 (113424/264690, TOPMED)
A=0.28320 (8002/28256, 14KJPN)
A=0.28473 (4772/16760, 8.3KJPN) (+ 16 more)
G=0.28763 (3176/11042, ALFA)
G=0.4852 (3107/6404, 1000G_30x)
G=0.4904 (2456/5008, 1000G)
G=0.4567 (2046/4480, Estonian)
G=0.4341 (1673/3854, ALSPAC)
G=0.4544 (1685/3708, TWINSUK)
A=0.3072 (900/2930, KOREAN)
A=0.3210 (588/1832, Korea1K)
G=0.425 (424/998, GoNL)
G=0.365 (219/600, NorthernSweden)
A=0.333 (134/402, SGDP_PRJ)
G=0.488 (161/330, HapMap)
G=0.435 (94/216, Qatari)
A=0.285 (61/214, Vietnamese)
G=0.42 (17/40, GENOME_DK)
A=0.38 (13/34, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RGS7 : 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	11042	A=0.71237	C=0.00000, G=0.28763
European	Sub	9206	A=0.6724	C=0.0000, G=0.3276
African	Sub	1186	A=0.9486	C=0.0000, G=0.0514
African Others	Sub	50	A=0.96	C=0.00, G=0.04
African American	Sub	1136	A=0.9481	C=0.0000, G=0.0519
Asian	Sub	14	A=0.79	C=0.00, G=0.21
East Asian	Sub	8	A=0.8	C=0.0, G=0.2
Other Asian	Sub	6	A=0.8	C=0.0, G=0.2
Latin American 1	Sub	50	A=1.00	C=0.00, G=0.00
Latin American 2	Sub	186	A=1.000	C=0.000, G=0.000
South Asian	Sub	38	A=0.95	C=0.00, G=0.05
Other	Sub	362	A=0.740	C=0.000, G=0.260

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	A=0.571484	G=0.428516
14KJPN	JAPANESE	Study-wide	28256	A=0.28320	G=0.71680
8.3KJPN	JAPANESE	Study-wide	16760	A=0.28473	G=0.71527
Allele Frequency Aggregator	Total	Global	11042	A=0.71237	C=0.00000, G=0.28763
Allele Frequency Aggregator	European	Sub	9206	A=0.6724	C=0.0000, G=0.3276
Allele Frequency Aggregator	African	Sub	1186	A=0.9486	C=0.0000, G=0.0514
Allele Frequency Aggregator	Other	Sub	362	A=0.740	C=0.000, G=0.260
Allele Frequency Aggregator	Latin American 2	Sub	186	A=1.000	C=0.000, G=0.000
Allele Frequency Aggregator	Latin American 1	Sub	50	A=1.00	C=0.00, G=0.00
Allele Frequency Aggregator	South Asian	Sub	38	A=0.95	C=0.00, G=0.05
Allele Frequency Aggregator	Asian	Sub	14	A=0.79	C=0.00, G=0.21
1000Genomes_30x	Global	Study-wide	6404	A=0.5147	C=0.0002, G=0.4852
1000Genomes_30x	African	Sub	1786	A=0.5952	C=0.0006, G=0.4043
1000Genomes_30x	Europe	Sub	1266	A=0.5964	C=0.0000, G=0.4036
1000Genomes_30x	South Asian	Sub	1202	A=0.5191	C=0.0000, G=0.4809
1000Genomes_30x	East Asian	Sub	1170	A=0.3085	C=0.0000, G=0.6915
1000Genomes_30x	American	Sub	980	A=0.503	C=0.000, G=0.497
1000Genomes	Global	Study-wide	5008	A=0.5096	G=0.4904
1000Genomes	African	Sub	1322	A=0.5968	G=0.4032
1000Genomes	East Asian	Sub	1008	A=0.2996	G=0.7004
1000Genomes	Europe	Sub	1006	A=0.5875	G=0.4125
1000Genomes	South Asian	Sub	978	A=0.525	G=0.475
1000Genomes	American	Sub	694	A=0.514	G=0.486
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.5433	G=0.4567
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.5659	G=0.4341
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.5456	G=0.4544
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.3072	G=0.6928
Korean Genome Project	KOREAN	Study-wide	1832	A=0.3210	G=0.6790
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.575	G=0.425
Northern Sweden	ACPOP	Study-wide	600	A=0.635	G=0.365
SGDP_PRJ	Global	Study-wide	402	A=0.333	G=0.667
HapMap	Global	Study-wide	330	A=0.512	G=0.488
HapMap	African	Sub	120	A=0.600	G=0.400
HapMap	American	Sub	120	A=0.592	G=0.408
HapMap	Asian	Sub	90	A=0.29	G=0.71
Qatari	Global	Study-wide	216	A=0.565	G=0.435
A Vietnamese Genetic Variation Database	Global	Study-wide	214	A=0.285	G=0.715
The Danish reference pan genome	Danish	Study-wide	40	A=0.57	G=0.42
Siberian	Global	Study-wide	34	A=0.38	G=0.62

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 1	NC_000001.11:g.240972145A>C
GRCh38.p14 chr 1	NC_000001.11:g.240972145A>G
GRCh37.p13 chr 1	NC_000001.10:g.241135445A>C
GRCh37.p13 chr 1	NC_000001.10:g.241135445A>G

Gene: RGS7, regulator of G protein signaling 7 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RGS7 transcript variant 2	NM_001282773.2:c.226+1093… NM_001282773.2:c.226+10934T>G	N/A	Intron Variant
RGS7 transcript variant 3	NM_001282775.2:c.226+1093… NM_001282775.2:c.226+10934T>G	N/A	Intron Variant
RGS7 transcript variant 4	NM_001282778.2:c.226+1093… NM_001282778.2:c.226+10934T>G	N/A	Intron Variant
RGS7 transcript variant 5	NM_001350113.2:c.148+1093… NM_001350113.2:c.148+10934T>G	N/A	Intron Variant
RGS7 transcript variant 6	NM_001350114.2:c.148+1093… NM_001350114.2:c.148+10934T>G	N/A	Intron Variant
RGS7 transcript variant 7	NM_001350115.2:c.148+1093… NM_001350115.2:c.148+10934T>G	N/A	Intron Variant
RGS7 transcript variant 8	NM_001350116.1:c.148+1093… NM_001350116.1:c.148+10934T>G	N/A	Intron Variant
RGS7 transcript variant 9	NM_001364886.1:c.226+1093… NM_001364886.1:c.226+10934T>G	N/A	Intron Variant
RGS7 transcript variant 10	NM_001374806.1:c.176-3543… NM_001374806.1:c.176-35439T>G	N/A	Intron Variant
RGS7 transcript variant 11	NM_001374807.1:c.176-3543… NM_001374807.1:c.176-35439T>G	N/A	Intron Variant
RGS7 transcript variant 12	NM_001374808.1:c.148+1093… NM_001374808.1:c.148+10934T>G	N/A	Intron Variant
RGS7 transcript variant 13	NM_001374809.1:c.-64+1093… NM_001374809.1:c.-64+10934T>G	N/A	Intron Variant
RGS7 transcript variant 14	NM_001374810.1:c.-64+1093… NM_001374810.1:c.-64+10934T>G	N/A	Intron Variant
RGS7 transcript variant 16	NM_001374811.1:c.226+1093… NM_001374811.1:c.226+10934T>G	N/A	Intron Variant
RGS7 transcript variant 15	NM_001374812.1:c.226+1093… NM_001374812.1:c.226+10934T>G	N/A	Intron Variant
RGS7 transcript variant 17	NM_001374813.1:c.-64+1093… NM_001374813.1:c.-64+10934T>G	N/A	Intron Variant
RGS7 transcript variant 18	NM_001374814.1:c.226+1093… NM_001374814.1:c.226+10934T>G	N/A	Intron Variant
RGS7 transcript variant 19	NM_001374815.1:c.226+1093… NM_001374815.1:c.226+10934T>G	N/A	Intron Variant
RGS7 transcript variant 20	NM_001374816.1:c.226+1093… NM_001374816.1:c.226+10934T>G	N/A	Intron Variant
RGS7 transcript variant 1	NM_002924.6:c.226+10934T>G	N/A	Intron Variant
RGS7 transcript variant X2	XM_017002009.2:c.148+1093… XM_017002009.2:c.148+10934T>G	N/A	Intron Variant
RGS7 transcript variant X1	XM_047426980.1:c.148+1093… XM_047426980.1:c.148+10934T>G	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	A=	C	G
GRCh38.p14 chr 1	NC_000001.11:g.240972145=	NC_000001.11:g.240972145A>C	NC_000001.11:g.240972145A>G
GRCh37.p13 chr 1	NC_000001.10:g.241135445=	NC_000001.10:g.241135445A>C	NC_000001.10:g.241135445A>G
RGS7 transcript variant 2	NM_001282773.2:c.226+10934=	NM_001282773.2:c.226+10934T>G	NM_001282773.2:c.226+10934T>C
RGS7 transcript variant 3	NM_001282775.2:c.226+10934=	NM_001282775.2:c.226+10934T>G	NM_001282775.2:c.226+10934T>C
RGS7 transcript variant 4	NM_001282778.2:c.226+10934=	NM_001282778.2:c.226+10934T>G	NM_001282778.2:c.226+10934T>C
RGS7 transcript variant 5	NM_001350113.2:c.148+10934=	NM_001350113.2:c.148+10934T>G	NM_001350113.2:c.148+10934T>C
RGS7 transcript variant 6	NM_001350114.2:c.148+10934=	NM_001350114.2:c.148+10934T>G	NM_001350114.2:c.148+10934T>C
RGS7 transcript variant 7	NM_001350115.2:c.148+10934=	NM_001350115.2:c.148+10934T>G	NM_001350115.2:c.148+10934T>C
RGS7 transcript variant 8	NM_001350116.1:c.148+10934=	NM_001350116.1:c.148+10934T>G	NM_001350116.1:c.148+10934T>C
RGS7 transcript variant 9	NM_001364886.1:c.226+10934=	NM_001364886.1:c.226+10934T>G	NM_001364886.1:c.226+10934T>C
RGS7 transcript variant 10	NM_001374806.1:c.176-35439=	NM_001374806.1:c.176-35439T>G	NM_001374806.1:c.176-35439T>C
RGS7 transcript variant 11	NM_001374807.1:c.176-35439=	NM_001374807.1:c.176-35439T>G	NM_001374807.1:c.176-35439T>C
RGS7 transcript variant 12	NM_001374808.1:c.148+10934=	NM_001374808.1:c.148+10934T>G	NM_001374808.1:c.148+10934T>C
RGS7 transcript variant 13	NM_001374809.1:c.-64+10934=	NM_001374809.1:c.-64+10934T>G	NM_001374809.1:c.-64+10934T>C
RGS7 transcript variant 14	NM_001374810.1:c.-64+10934=	NM_001374810.1:c.-64+10934T>G	NM_001374810.1:c.-64+10934T>C
RGS7 transcript variant 16	NM_001374811.1:c.226+10934=	NM_001374811.1:c.226+10934T>G	NM_001374811.1:c.226+10934T>C
RGS7 transcript variant 15	NM_001374812.1:c.226+10934=	NM_001374812.1:c.226+10934T>G	NM_001374812.1:c.226+10934T>C
RGS7 transcript variant 17	NM_001374813.1:c.-64+10934=	NM_001374813.1:c.-64+10934T>G	NM_001374813.1:c.-64+10934T>C
RGS7 transcript variant 18	NM_001374814.1:c.226+10934=	NM_001374814.1:c.226+10934T>G	NM_001374814.1:c.226+10934T>C
RGS7 transcript variant 19	NM_001374815.1:c.226+10934=	NM_001374815.1:c.226+10934T>G	NM_001374815.1:c.226+10934T>C
RGS7 transcript variant 20	NM_001374816.1:c.226+10934=	NM_001374816.1:c.226+10934T>G	NM_001374816.1:c.226+10934T>C
RGS7 transcript	NM_002924.4:c.226+10934=	NM_002924.4:c.226+10934T>G	NM_002924.4:c.226+10934T>C
RGS7 transcript variant 1	NM_002924.6:c.226+10934=	NM_002924.6:c.226+10934T>G	NM_002924.6:c.226+10934T>C
RGS7 transcript variant X1	XM_005273218.1:c.226+10934=	XM_005273218.1:c.226+10934T>G	XM_005273218.1:c.226+10934T>C
RGS7 transcript variant X2	XM_005273219.1:c.226+10934=	XM_005273219.1:c.226+10934T>G	XM_005273219.1:c.226+10934T>C
RGS7 transcript variant X3	XM_005273220.1:c.226+10934=	XM_005273220.1:c.226+10934T>G	XM_005273220.1:c.226+10934T>C
RGS7 transcript variant X4	XM_005273221.1:c.148+10934=	XM_005273221.1:c.148+10934T>G	XM_005273221.1:c.148+10934T>C
RGS7 transcript variant X5	XM_005273222.1:c.226+10934=	XM_005273222.1:c.226+10934T>G	XM_005273222.1:c.226+10934T>C
RGS7 transcript variant X6	XM_005273223.1:c.226+10934=	XM_005273223.1:c.226+10934T>G	XM_005273223.1:c.226+10934T>C
RGS7 transcript variant X2	XM_017002009.2:c.148+10934=	XM_017002009.2:c.148+10934T>G	XM_017002009.2:c.148+10934T>C
RGS7 transcript variant X1	XM_047426980.1:c.148+10934=	XM_047426980.1:c.148+10934T>G	XM_047426980.1:c.148+10934T>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#.

69 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss6415038	Feb 20, 2003 (111)
2	PERLEGEN	ss24713740	Sep 20, 2004 (123)
3	BCMHGSC_JDW	ss88032092	Mar 23, 2008 (129)
4	HUMANGENOME_JCVI	ss99301612	Feb 04, 2009 (130)
5	BGI	ss106644301	Feb 04, 2009 (130)
6	1000GENOMES	ss109091133	Jan 23, 2009 (130)
7	1000GENOMES	ss112036399	Jan 25, 2009 (130)
8	ENSEMBL	ss138184862	Dec 01, 2009 (131)
9	ENSEMBL	ss139016478	Dec 01, 2009 (131)
10	GMI	ss156502024	Dec 01, 2009 (131)
11	COMPLETE_GENOMICS	ss165538074	Jul 04, 2010 (132)
12	COMPLETE_GENOMICS	ss165934864	Jul 04, 2010 (132)
13	BUSHMAN	ss199837380	Jul 04, 2010 (132)
14	1000GENOMES	ss218977977	Jul 14, 2010 (132)
15	1000GENOMES	ss230974515	Jul 14, 2010 (132)
16	1000GENOMES	ss238574310	Jul 15, 2010 (132)
17	GMI	ss276288967	May 04, 2012 (137)
18	PJP	ss290770713	May 09, 2011 (134)
19	TISHKOFF	ss555253336	Apr 25, 2013 (138)
20	SSMP	ss648827556	Apr 25, 2013 (138)
21	EVA-GONL	ss976330867	Aug 21, 2014 (142)
22	JMKIDD_LAB	ss1068742729	Aug 21, 2014 (142)
23	1000GENOMES	ss1295336298	Aug 21, 2014 (142)
24	DDI	ss1426167360	Apr 01, 2015 (144)
25	EVA_GENOME_DK	ss1574799185	Apr 01, 2015 (144)
26	EVA_DECODE	ss1585735155	Apr 01, 2015 (144)
27	EVA_UK10K_ALSPAC	ss1602508405	Apr 01, 2015 (144)
28	EVA_UK10K_TWINSUK	ss1645502438	Apr 01, 2015 (144)
29	HAMMER_LAB	ss1795997936	Sep 08, 2015 (146)
30	WEILL_CORNELL_DGM	ss1919552509	Feb 12, 2016 (147)
31	GENOMED	ss1967017936	Jul 19, 2016 (147)
32	JJLAB	ss2020303891	Sep 14, 2016 (149)
33	USC_VALOUEV	ss2148341852	Dec 20, 2016 (150)
34	HUMAN_LONGEVITY	ss2171498631	Dec 20, 2016 (150)
35	SYSTEMSBIOZJU	ss2624665364	Nov 08, 2017 (151)
36	GRF	ss2698345328	Nov 08, 2017 (151)
37	GNOMAD	ss2768141400	Nov 08, 2017 (151)
38	SWEGEN	ss2988736770	Nov 08, 2017 (151)
39	BIOINF_KMB_FNS_UNIBA	ss3023914315	Nov 08, 2017 (151)
40	CSHL	ss3343996334	Nov 08, 2017 (151)
41	URBANLAB	ss3646926663	Oct 11, 2018 (152)
42	EGCUT_WGS	ss3656697935	Jul 12, 2019 (153)
43	EVA_DECODE	ss3688975575	Jul 12, 2019 (153)
44	ACPOP	ss3728018536	Jul 12, 2019 (153)
45	EVA	ss3747553153	Jul 12, 2019 (153)
46	PACBIO	ss3783736827	Jul 12, 2019 (153)
47	PACBIO	ss3789341724	Jul 12, 2019 (153)
48	PACBIO	ss3794214181	Jul 12, 2019 (153)
49	KHV_HUMAN_GENOMES	ss3800556573	Jul 12, 2019 (153)
50	EVA	ss3826737787	Apr 25, 2020 (154)
51	EVA	ss3836771747	Apr 25, 2020 (154)
52	EVA	ss3842184696	Apr 25, 2020 (154)
53	SGDP_PRJ	ss3851261454	Apr 25, 2020 (154)
54	KRGDB	ss3896621703	Apr 25, 2020 (154)
55	KOGIC	ss3946845535	Apr 25, 2020 (154)
56	TOPMED	ss4489490614	Apr 25, 2021 (155)
57	TOMMO_GENOMICS	ss5149216895	Apr 25, 2021 (155)
58	1000G_HIGH_COVERAGE	ss5246398793	Oct 17, 2022 (156)
59	EVA	ss5325885963	Oct 17, 2022 (156)
60	HUGCELL_USP	ss5446778517	Oct 17, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5520795910	Oct 17, 2022 (156)
62	SANFORD_IMAGENETICS	ss5627793003	Oct 17, 2022 (156)
63	TOMMO_GENOMICS	ss5677204121	Oct 17, 2022 (156)
64	YY_MCH	ss5801795289	Oct 17, 2022 (156)
65	EVA	ss5833508698	Oct 17, 2022 (156)
66	EVA	ss5849365627	Oct 17, 2022 (156)
67	EVA	ss5912666221	Oct 17, 2022 (156)
68	EVA	ss5939643551	Oct 17, 2022 (156)
69	EVA	ss5980026692	Oct 17, 2022 (156)
70	1000Genomes	NC_000001.10 - 241135445	Oct 11, 2018 (152)
71	1000Genomes_30x	NC_000001.11 - 240972145	Oct 17, 2022 (156)
72	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 241135445	Oct 11, 2018 (152)
73	Genetic variation in the Estonian population	NC_000001.10 - 241135445	Oct 11, 2018 (152)
74	The Danish reference pan genome	NC_000001.10 - 241135445	Apr 25, 2020 (154)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 44479927 (NC_000001.11:240972144:A:C 8/140084) Row 44479928 (NC_000001.11:240972144:A:G 59931/140018)	-	Apr 25, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 44479927 (NC_000001.11:240972144:A:C 8/140084) Row 44479928 (NC_000001.11:240972144:A:G 59931/140018)	-	Apr 25, 2021 (155)
77	Genome of the Netherlands Release 5	NC_000001.10 - 241135445	Apr 25, 2020 (154)
78	HapMap	NC_000001.11 - 240972145	Apr 25, 2020 (154)
79	KOREAN population from KRGDB	NC_000001.10 - 241135445	Apr 25, 2020 (154)
80	Korean Genome Project	NC_000001.11 - 240972145	Apr 25, 2020 (154)
81	Northern Sweden	NC_000001.10 - 241135445	Jul 12, 2019 (153)
82	Qatari	NC_000001.10 - 241135445	Apr 25, 2020 (154)
83	SGDP_PRJ	NC_000001.10 - 241135445	Apr 25, 2020 (154)
84	Siberian	NC_000001.10 - 241135445	Apr 25, 2020 (154)
85	8.3KJPN	NC_000001.10 - 241135445	Apr 25, 2021 (155)
86	14KJPN	NC_000001.11 - 240972145	Oct 17, 2022 (156)
87	TopMed	NC_000001.11 - 240972145	Apr 25, 2021 (155)
88	UK 10K study - Twins	NC_000001.10 - 241135445	Oct 11, 2018 (152)
89	A Vietnamese Genetic Variation Database	NC_000001.10 - 241135445	Jul 12, 2019 (153)
90	ALFA	NC_000001.11 - 240972145	Apr 25, 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)
rs17823775	Oct 07, 2004 (123)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss2768141400, ss5627793003	NC_000001.10:241135444:A:C	NC_000001.11:240972144:A:C	(self)
8321845, 6336970515, ss2171498631, ss5520795910	NC_000001.11:240972144:A:C	NC_000001.11:240972144:A:C	(self)
ss88032092, ss109091133, ss112036399, ss165538074, ss165934864, ss199837380, ss276288967, ss290770713, ss1585735155	NC_000001.9:239202067:A:G	NC_000001.11:240972144:A:G	(self)
6216523, 3444667, 2436183, 1960374, 1508954, 3799097, 1303401, 1594439, 3278434, 858206, 7186202, 3444667, 751231, ss218977977, ss230974515, ss238574310, ss555253336, ss648827556, ss976330867, ss1068742729, ss1295336298, ss1426167360, ss1574799185, ss1602508405, ss1645502438, ss1795997936, ss1919552509, ss1967017936, ss2020303891, ss2148341852, ss2624665364, ss2698345328, ss2768141400, ss2988736770, ss3343996334, ss3656697935, ss3728018536, ss3747553153, ss3783736827, ss3789341724, ss3794214181, ss3826737787, ss3836771747, ss3851261454, ss3896621703, ss5149216895, ss5325885963, ss5627793003, ss5833508698, ss5939643551, ss5980026692	NC_000001.10:241135444:A:G	NC_000001.11:240972144:A:G	(self)
8321845, 306018, 3223536, 11041225, 53096949, 6336970515, ss2171498631, ss3023914315, ss3646926663, ss3688975575, ss3800556573, ss3842184696, ss3946845535, ss4489490614, ss5246398793, ss5446778517, ss5520795910, ss5677204121, ss5801795289, ss5849365627, ss5912666221	NC_000001.11:240972144:A:G	NC_000001.11:240972144:A:G	(self)
ss6415038, ss24713740, ss99301612, ss106644301, ss138184862, ss139016478, ss156502024	NT_167186.1:34653223:A:G	NC_000001.11:240972144:A: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 rs4660016

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

rs4660016