Name: rs3887211
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.

rs3887211

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:47807585 (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: G=0.360497 (95420/264690, TOPMED)
G=0.365876 (75350/205944, ALFA)
G=0.355302 (49743/140002, GnomAD) (+ 19 more)
G=0.31563 (8919/28258, 14KJPN)
G=0.31185 (5226/16758, 8.3KJPN)
G=0.3495 (2238/6404, 1000G_30x)
G=0.3431 (1718/5008, 1000G)
G=0.3136 (1405/4480, Estonian)
G=0.3874 (1493/3854, ALSPAC)
G=0.3657 (1356/3708, TWINSUK)
G=0.3461 (1014/2930, KOREAN)
G=0.3311 (690/2084, HGDP_Stanford)
G=0.3452 (651/1886, HapMap)
G=0.3439 (630/1832, Korea1K)
G=0.435 (434/998, GoNL)
G=0.397 (238/600, NorthernSweden)
G=0.238 (110/462, SGDP_PRJ)
G=0.375 (81/216, Qatari)
G=0.463 (99/214, Vietnamese)
G=0.42 (40/96, Ancient Sardinia)
G=0.17 (8/48, Siberian)
G=0.45 (18/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PKD1L1 : Intron Variant
PKD1L1-AS1 : 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	206038	G=0.365918	A=0.634082
European	Sub	174994	G=0.364635	A=0.635365
African	Sub	7768	G=0.3227	A=0.6773
African Others	Sub	276	G=0.333	A=0.667
African American	Sub	7492	G=0.3223	A=0.6777
Asian	Sub	748	G=0.377	A=0.623
East Asian	Sub	572	G=0.383	A=0.617
Other Asian	Sub	176	G=0.358	A=0.642
Latin American 1	Sub	990	G=0.412	A=0.588
Latin American 2	Sub	9034	G=0.4355	A=0.5645
South Asian	Sub	5052	G=0.3157	A=0.6843
Other	Sub	7452	G=0.3835	A=0.6165

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=0.360497	A=0.639503
Allele Frequency Aggregator	Total	Global	205944	G=0.365876	A=0.634124
Allele Frequency Aggregator	European	Sub	174918	G=0.364588	A=0.635412
Allele Frequency Aggregator	Latin American 2	Sub	9034	G=0.4355	A=0.5645
Allele Frequency Aggregator	African	Sub	7768	G=0.3227	A=0.6773
Allele Frequency Aggregator	Other	Sub	7434	G=0.3835	A=0.6165
Allele Frequency Aggregator	South Asian	Sub	5052	G=0.3157	A=0.6843
Allele Frequency Aggregator	Latin American 1	Sub	990	G=0.412	A=0.588
Allele Frequency Aggregator	Asian	Sub	748	G=0.377	A=0.623
gnomAD - Genomes	Global	Study-wide	140002	G=0.355302	A=0.644698
gnomAD - Genomes	European	Sub	75832	G=0.36909	A=0.63091
gnomAD - Genomes	African	Sub	41938	G=0.32193	A=0.67807
gnomAD - Genomes	American	Sub	13642	G=0.37495	A=0.62505
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	G=0.3620	A=0.6380
gnomAD - Genomes	East Asian	Sub	3120	G=0.3740	A=0.6260
gnomAD - Genomes	Other	Sub	2152	G=0.3578	A=0.6422
14KJPN	JAPANESE	Study-wide	28258	G=0.31563	A=0.68437
8.3KJPN	JAPANESE	Study-wide	16758	G=0.31185	A=0.68815
1000Genomes_30x	Global	Study-wide	6404	G=0.3495	A=0.6505
1000Genomes_30x	African	Sub	1786	G=0.3147	A=0.6853
1000Genomes_30x	Europe	Sub	1266	G=0.3720	A=0.6280
1000Genomes_30x	South Asian	Sub	1202	G=0.3062	A=0.6938
1000Genomes_30x	East Asian	Sub	1170	G=0.3726	A=0.6274
1000Genomes_30x	American	Sub	980	G=0.409	A=0.591
1000Genomes	Global	Study-wide	5008	G=0.3431	A=0.6569
1000Genomes	African	Sub	1322	G=0.3139	A=0.6861
1000Genomes	East Asian	Sub	1008	G=0.3651	A=0.6349
1000Genomes	Europe	Sub	1006	G=0.3608	A=0.6392
1000Genomes	South Asian	Sub	978	G=0.297	A=0.703
1000Genomes	American	Sub	694	G=0.406	A=0.594
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.3136	A=0.6864
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.3874	A=0.6126
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.3657	A=0.6343
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.3461	A=0.6539, C=0.0000, T=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	G=0.3311	A=0.6689
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	G=0.323	A=0.677
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	G=0.302	A=0.698
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.377	A=0.623
HGDP-CEPH-db Supplement 1	Europe	Sub	320	G=0.331	A=0.669
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.236	A=0.764
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.505	A=0.495
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.12	A=0.88
HapMap	Global	Study-wide	1886	G=0.3452	A=0.6548
HapMap	American	Sub	768	G=0.385	A=0.615
HapMap	African	Sub	690	G=0.293	A=0.707
HapMap	Asian	Sub	252	G=0.341	A=0.659
HapMap	Europe	Sub	176	G=0.381	A=0.619
Korean Genome Project	KOREAN	Study-wide	1832	G=0.3439	A=0.6561
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.435	A=0.565
Northern Sweden	ACPOP	Study-wide	600	G=0.397	A=0.603
SGDP_PRJ	Global	Study-wide	462	G=0.238	A=0.762
Qatari	Global	Study-wide	216	G=0.375	A=0.625
A Vietnamese Genetic Variation Database	Global	Study-wide	214	G=0.463	A=0.537
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	96	G=0.42	A=0.58
Siberian	Global	Study-wide	48	G=0.17	A=0.83
The Danish reference pan genome	Danish	Study-wide	40	G=0.45	A=0.55

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 7	NC_000007.14:g.47807585G>A
GRCh38.p14 chr 7	NC_000007.14:g.47807585G>C
GRCh38.p14 chr 7	NC_000007.14:g.47807585G>T
GRCh37.p13 chr 7	NC_000007.13:g.47847183G>A
GRCh37.p13 chr 7	NC_000007.13:g.47847183G>C
GRCh37.p13 chr 7	NC_000007.13:g.47847183G>T
PKD1L1 RefSeqGene	NG_052801.1:g.156038C>T
PKD1L1 RefSeqGene	NG_052801.1:g.156038C>G
PKD1L1 RefSeqGene	NG_052801.1:g.156038C>A

Gene: PKD1L1, polycystin 1 like 1, transient receptor potential channel interacting (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PKD1L1 transcript	NM_138295.5:c.7827+662C>T	N/A	Intron Variant
PKD1L1 transcript variant X1	XM_017011798.3:c.8004+662… XM_017011798.3:c.8004+662C>T	N/A	Intron Variant

Gene: PKD1L1-AS1, PKD1L1 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PKD1L1-AS1 transcript variant 1	NR_161268.1:n.	N/A	Intron Variant
PKD1L1-AS1 transcript variant 2	NR_161269.1:n.	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	G=	A	C	T
GRCh38.p14 chr 7	NC_000007.14:g.47807585=	NC_000007.14:g.47807585G>A	NC_000007.14:g.47807585G>C	NC_000007.14:g.47807585G>T
GRCh37.p13 chr 7	NC_000007.13:g.47847183=	NC_000007.13:g.47847183G>A	NC_000007.13:g.47847183G>C	NC_000007.13:g.47847183G>T
PKD1L1 RefSeqGene	NG_052801.1:g.156038=	NG_052801.1:g.156038C>T	NG_052801.1:g.156038C>G	NG_052801.1:g.156038C>A
C7orf69 transcript variant 1	NM_025031.2:c.109-10441=	NM_025031.2:c.109-10441G>A	NM_025031.2:c.109-10441G>C	NM_025031.2:c.109-10441G>T
PKD1L1 transcript	NM_138295.3:c.7827+662=	NM_138295.3:c.7827+662C>T	NM_138295.3:c.7827+662C>G	NM_138295.3:c.7827+662C>A
PKD1L1 transcript	NM_138295.5:c.7827+662=	NM_138295.5:c.7827+662C>T	NM_138295.5:c.7827+662C>G	NM_138295.5:c.7827+662C>A
PKD1L1 transcript variant X1	XM_017011798.3:c.8004+662=	XM_017011798.3:c.8004+662C>T	XM_017011798.3:c.8004+662C>G	XM_017011798.3:c.8004+662C>A

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#.

129 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss69702	Oct 10, 2002 (108)
2	SC_JCM	ss5701445	Feb 20, 2003 (111)
3	BCM_SSAHASNP	ss10417245	Jul 11, 2003 (116)
4	WI_SSAHASNP	ss11905809	Jul 11, 2003 (116)
5	CSHL-HAPMAP	ss17942070	Feb 27, 2004 (120)
6	SSAHASNP	ss22567355	Apr 05, 2004 (121)
7	SSAHASNP	ss22948488	Apr 05, 2004 (121)
8	PERLEGEN	ss24184178	Sep 20, 2004 (123)
9	ABI	ss44807342	Mar 14, 2006 (126)
10	ILLUMINA	ss67309893	Dec 01, 2006 (127)
11	ILLUMINA	ss67715501	Dec 01, 2006 (127)
12	ILLUMINA	ss68223713	Dec 12, 2006 (127)
13	PERLEGEN	ss69015478	May 18, 2007 (127)
14	ILLUMINA	ss70788544	May 24, 2008 (130)
15	ILLUMINA	ss71365687	May 18, 2007 (127)
16	ILLUMINA	ss75653327	Dec 06, 2007 (129)
17	AFFY	ss76807262	Dec 08, 2007 (130)
18	HGSV	ss81612500	Dec 15, 2007 (130)
19	KRIBB_YJKIM	ss84210988	Dec 15, 2007 (130)
20	BCMHGSC_JDW	ss93673427	Mar 24, 2008 (129)
21	BGI	ss104424951	Dec 01, 2009 (131)
22	1000GENOMES	ss111940621	Jan 25, 2009 (130)
23	1000GENOMES	ss113703968	Jan 25, 2009 (130)
24	ILLUMINA-UK	ss116066441	Feb 14, 2009 (130)
25	ENSEMBL	ss142697801	Dec 01, 2009 (131)
26	ILLUMINA	ss154276505	Dec 01, 2009 (131)
27	GMI	ss154741635	Dec 01, 2009 (131)
28	ILLUMINA	ss159453191	Dec 01, 2009 (131)
29	ILLUMINA	ss160652748	Dec 01, 2009 (131)
30	COMPLETE_GENOMICS	ss162291821	Jul 04, 2010 (132)
31	COMPLETE_GENOMICS	ss164169082	Jul 04, 2010 (132)
32	ILLUMINA	ss173667018	Jul 04, 2010 (132)
33	BUSHMAN	ss203283803	Jul 04, 2010 (132)
34	BCM-HGSC-SUB	ss208130581	Jul 04, 2010 (132)
35	1000GENOMES	ss223057469	Jul 14, 2010 (132)
36	1000GENOMES	ss233962275	Jul 15, 2010 (132)
37	1000GENOMES	ss240919141	Jul 15, 2010 (132)
38	BL	ss254247283	May 09, 2011 (134)
39	GMI	ss279293130	May 04, 2012 (137)
40	GMI	ss285621337	Apr 25, 2013 (138)
41	PJP	ss293861813	May 09, 2011 (134)
42	ILLUMINA	ss480866990	May 04, 2012 (137)
43	ILLUMINA	ss480885647	May 04, 2012 (137)
44	ILLUMINA	ss481825586	Sep 08, 2015 (146)
45	ILLUMINA	ss485228603	May 04, 2012 (137)
46	ILLUMINA	ss537206003	Sep 08, 2015 (146)
47	TISHKOFF	ss559982510	Apr 25, 2013 (138)
48	SSMP	ss654341794	Apr 25, 2013 (138)
49	ILLUMINA	ss778899876	Sep 08, 2015 (146)
50	ILLUMINA	ss783060245	Sep 08, 2015 (146)
51	ILLUMINA	ss784018365	Sep 08, 2015 (146)
52	ILLUMINA	ss832318208	Sep 08, 2015 (146)
53	ILLUMINA	ss832964724	Jul 13, 2019 (153)
54	ILLUMINA	ss834361113	Sep 08, 2015 (146)
55	EVA-GONL	ss984239540	Aug 21, 2014 (142)
56	JMKIDD_LAB	ss1074581151	Aug 21, 2014 (142)
57	1000GENOMES	ss1324992508	Aug 21, 2014 (142)
58	DDI	ss1431111732	Apr 01, 2015 (144)
59	EVA_GENOME_DK	ss1582186730	Apr 01, 2015 (144)
60	EVA_DECODE	ss1593816414	Apr 01, 2015 (144)
61	EVA_UK10K_ALSPAC	ss1618140615	Apr 01, 2015 (144)
62	EVA_UK10K_TWINSUK	ss1661134648	Apr 01, 2015 (144)
63	EVA_SVP	ss1712953409	Apr 01, 2015 (144)
64	ILLUMINA	ss1752688070	Sep 08, 2015 (146)
65	HAMMER_LAB	ss1804987577	Sep 08, 2015 (146)
66	WEILL_CORNELL_DGM	ss1927483998	Feb 12, 2016 (147)
67	GENOMED	ss1970691855	Jul 19, 2016 (147)
68	JJLAB	ss2024424825	Sep 14, 2016 (149)
69	ILLUMINA	ss2094831140	Dec 20, 2016 (150)
70	ILLUMINA	ss2095198410	Dec 20, 2016 (150)
71	USC_VALOUEV	ss2152621421	Dec 20, 2016 (150)
72	HUMAN_LONGEVITY	ss2293764303	Dec 20, 2016 (150)
73	SYSTEMSBIOZJU	ss2626699449	Nov 08, 2017 (151)
74	ILLUMINA	ss2634602819	Nov 08, 2017 (151)
75	GRF	ss2708284966	Nov 08, 2017 (151)
76	GNOMAD	ss2852759625	Nov 08, 2017 (151)
77	AFFY	ss2985406535	Nov 08, 2017 (151)
78	AFFY	ss2986037859	Nov 08, 2017 (151)
79	SWEGEN	ss3001061473	Nov 08, 2017 (151)
80	BIOINF_KMB_FNS_UNIBA	ss3026007455	Nov 08, 2017 (151)
81	CSHL	ss3347567573	Nov 08, 2017 (151)
82	ILLUMINA	ss3629811256	Oct 12, 2018 (152)
83	ILLUMINA	ss3632510441	Oct 12, 2018 (152)
84	ILLUMINA	ss3633462570	Oct 12, 2018 (152)
85	ILLUMINA	ss3634187457	Oct 12, 2018 (152)
86	ILLUMINA	ss3635120479	Oct 12, 2018 (152)
87	ILLUMINA	ss3635867301	Oct 12, 2018 (152)
88	ILLUMINA	ss3636852629	Oct 12, 2018 (152)
89	ILLUMINA	ss3637620268	Oct 12, 2018 (152)
90	ILLUMINA	ss3638696426	Oct 12, 2018 (152)
91	ILLUMINA	ss3639350929	Oct 12, 2018 (152)
92	ILLUMINA	ss3639970207	Oct 12, 2018 (152)
93	ILLUMINA	ss3640827772	Oct 12, 2018 (152)
94	ILLUMINA	ss3643632320	Oct 12, 2018 (152)
95	ILLUMINA	ss3644014379	Oct 12, 2018 (152)
96	URBANLAB	ss3648622457	Oct 12, 2018 (152)
97	ILLUMINA	ss3653263745	Oct 12, 2018 (152)
98	ILLUMINA	ss3654167269	Oct 12, 2018 (152)
99	EGCUT_WGS	ss3668982864	Jul 13, 2019 (153)
100	EVA_DECODE	ss3719626677	Jul 13, 2019 (153)
101	ACPOP	ss3734599979	Jul 13, 2019 (153)
102	ILLUMINA	ss3745420532	Jul 13, 2019 (153)
103	EVA	ss3766521029	Jul 13, 2019 (153)
104	ILLUMINA	ss3772913475	Jul 13, 2019 (153)
105	KHV_HUMAN_GENOMES	ss3809681328	Jul 13, 2019 (153)
106	EVA	ss3830554931	Apr 26, 2020 (154)
107	EVA	ss3838765627	Apr 26, 2020 (154)
108	EVA	ss3844217731	Apr 26, 2020 (154)
109	HGDP	ss3847876227	Apr 26, 2020 (154)
110	SGDP_PRJ	ss3867195952	Apr 26, 2020 (154)
111	KRGDB	ss3914269532	Apr 26, 2020 (154)
112	KOGIC	ss3961401944	Apr 26, 2020 (154)
113	EVA	ss3985295250	Apr 26, 2021 (155)
114	EVA	ss4017335159	Apr 26, 2021 (155)
115	TOPMED	ss4744805188	Apr 26, 2021 (155)
116	TOMMO_GENOMICS	ss5183000790	Apr 26, 2021 (155)
117	1000G_HIGH_COVERAGE	ss5272757917	Oct 14, 2022 (156)
118	EVA	ss5315246364	Oct 14, 2022 (156)
119	EVA	ss5373342017	Oct 14, 2022 (156)
120	HUGCELL_USP	ss5469943227	Oct 14, 2022 (156)
121	1000G_HIGH_COVERAGE	ss5560864904	Oct 14, 2022 (156)
122	SANFORD_IMAGENETICS	ss5642880365	Oct 14, 2022 (156)
123	TOMMO_GENOMICS	ss5722793641	Oct 14, 2022 (156)
124	EVA	ss5799724252	Oct 14, 2022 (156)
125	YY_MCH	ss5808570495	Oct 14, 2022 (156)
126	EVA	ss5822775051	Oct 14, 2022 (156)
127	EVA	ss5855878518	Oct 14, 2022 (156)
128	EVA	ss5858771228	Oct 14, 2022 (156)
129	EVA	ss5972095134	Oct 14, 2022 (156)
130	1000Genomes	NC_000007.13 - 47847183	Oct 12, 2018 (152)
131	1000Genomes_30x	NC_000007.14 - 47807585	Oct 14, 2022 (156)
132	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 47847183	Oct 12, 2018 (152)
133	Genetic variation in the Estonian population	NC_000007.13 - 47847183	Oct 12, 2018 (152)
134	The Danish reference pan genome	NC_000007.13 - 47847183	Apr 26, 2020 (154)
135	gnomAD - Genomes	NC_000007.14 - 47807585	Apr 26, 2021 (155)
136	Genome of the Netherlands Release 5	NC_000007.13 - 47847183	Apr 26, 2020 (154)
137	HGDP-CEPH-db Supplement 1	NC_000007.12 - 47813708	Apr 26, 2020 (154)
138	HapMap	NC_000007.14 - 47807585	Apr 26, 2020 (154)
139	KOREAN population from KRGDB	NC_000007.13 - 47847183	Apr 26, 2020 (154)
140	Korean Genome Project	NC_000007.14 - 47807585	Apr 26, 2020 (154)
141	Northern Sweden	NC_000007.13 - 47847183	Jul 13, 2019 (153)
142	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000007.13 - 47847183	Apr 26, 2021 (155)
143	Qatari	NC_000007.13 - 47847183	Apr 26, 2020 (154)
144	SGDP_PRJ	NC_000007.13 - 47847183	Apr 26, 2020 (154)
145	Siberian	NC_000007.13 - 47847183	Apr 26, 2020 (154)
146	8.3KJPN	NC_000007.13 - 47847183	Apr 26, 2021 (155)
147	14KJPN	NC_000007.14 - 47807585	Oct 14, 2022 (156)
148	TopMed	NC_000007.14 - 47807585	Apr 26, 2021 (155)
149	UK 10K study - Twins	NC_000007.13 - 47847183	Oct 12, 2018 (152)
150	A Vietnamese Genetic Variation Database	NC_000007.13 - 47847183	Jul 13, 2019 (153)
151	ALFA	NC_000007.14 - 47807585	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)
rs17659745	Oct 08, 2004 (123)
rs56590123	May 24, 2008 (130)
rs58209172	May 24, 2008 (130)
rs386588545	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss81612500, ss3639350929, ss3639970207, ss3644014379	NC_000007.11:47620422:G:A	NC_000007.14:47807584:G:A	(self)
554119, ss76807262, ss93673427, ss111940621, ss113703968, ss116066441, ss162291821, ss164169082, ss203283803, ss208130581, ss254247283, ss279293130, ss285621337, ss293861813, ss480866990, ss1593816414, ss1712953409, ss3643632320, ss3847876227	NC_000007.12:47813707:G:A	NC_000007.14:47807584:G:A	(self)
36957306, 20610947, 14721112, 8351669, 9190791, 21446926, 7884844, 521177, 9525928, 19212932, 5137775, 40970097, 20610947, 4593021, ss223057469, ss233962275, ss240919141, ss480885647, ss481825586, ss485228603, ss537206003, ss559982510, ss654341794, ss778899876, ss783060245, ss784018365, ss832318208, ss832964724, ss834361113, ss984239540, ss1074581151, ss1324992508, ss1431111732, ss1582186730, ss1618140615, ss1661134648, ss1752688070, ss1804987577, ss1927483998, ss1970691855, ss2024424825, ss2094831140, ss2095198410, ss2152621421, ss2626699449, ss2634602819, ss2708284966, ss2852759625, ss2985406535, ss2986037859, ss3001061473, ss3347567573, ss3629811256, ss3632510441, ss3633462570, ss3634187457, ss3635120479, ss3635867301, ss3636852629, ss3637620268, ss3638696426, ss3640827772, ss3653263745, ss3654167269, ss3668982864, ss3734599979, ss3745420532, ss3766521029, ss3772913475, ss3830554931, ss3838765627, ss3867195952, ss3914269532, ss3985295250, ss4017335159, ss5183000790, ss5315246364, ss5373342017, ss5642880365, ss5799724252, ss5822775051, ss5972095134	NC_000007.13:47847182:G:A	NC_000007.14:47807584:G:A	(self)
48390839, 260514091, 3394913, 17779945, 56630745, 582182747, 11562501336, ss2293764303, ss3026007455, ss3648622457, ss3719626677, ss3809681328, ss3844217731, ss3961401944, ss4744805188, ss5272757917, ss5469943227, ss5560864904, ss5722793641, ss5808570495, ss5855878518, ss5858771228	NC_000007.14:47807584:G:A	NC_000007.14:47807584:G:A	(self)
ss10417245, ss11905809	NT_007819.13:47139298:G:A	NC_000007.14:47807584:G:A	(self)
ss17942070, ss22567355, ss22948488	NT_007819.14:47139298:G:A	NC_000007.14:47807584:G:A	(self)
ss69702, ss5701445, ss24184178, ss44807342, ss67309893, ss67715501, ss68223713, ss69015478, ss70788544, ss71365687, ss75653327, ss84210988, ss104424951, ss142697801, ss154276505, ss154741635, ss159453191, ss160652748, ss173667018	NT_007819.17:47837182:G:A	NC_000007.14:47807584:G:A	(self)
21446926, ss3914269532	NC_000007.13:47847182:G:C	NC_000007.14:47807584:G:C	(self)
21446926, ss3914269532	NC_000007.13:47847182:G:T	NC_000007.14:47807584: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 rs3887211

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

rs3887211