Name: rs2047163
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.

rs2047163

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:218535261 (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: C>A
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.248683 (77440/311400, ALFA)
A=0.218762 (57904/264690, TOPMED)
A=0.217550 (30433/139890, GnomAD) (+ 22 more)
A=0.21780 (17141/78700, PAGE_STUDY)
A=0.35352 (9989/28256, 14KJPN)
A=0.35555 (5959/16760, 8.3KJPN)
A=0.2249 (1440/6404, 1000G_30x)
A=0.2312 (1158/5008, 1000G)
A=0.2824 (1265/4480, Estonian)
A=0.2429 (936/3854, ALSPAC)
A=0.2389 (886/3708, TWINSUK)
A=0.3535 (1033/2922, KOREAN)
A=0.3148 (656/2084, HGDP_Stanford)
A=0.2172 (411/1892, HapMap)
A=0.3663 (671/1832, Korea1K)
A=0.271 (270/998, GoNL)
A=0.322 (254/788, PRJEB37584)
A=0.326 (204/626, Chileans)
A=0.297 (178/600, NorthernSweden)
C=0.393 (95/242, SGDP_PRJ)
A=0.181 (39/216, Qatari)
A=0.278 (59/212, Vietnamese)
A=0.14 (12/86, Ancient Sardinia)
A=0.17 (7/40, GENOME_DK)
C=0.45 (17/38, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	316436	C=0.751792	A=0.248208
European	Sub	275880	C=0.752204	A=0.247796
African	Sub	10204	C=0.88044	A=0.11956
African Others	Sub	384	C=0.919	A=0.081
African American	Sub	9820	C=0.8789	A=0.1211
Asian	Sub	3988	C=0.6908	A=0.3092
East Asian	Sub	3210	C=0.6636	A=0.3364
Other Asian	Sub	778	C=0.803	A=0.197
Latin American 1	Sub	1276	C=0.7578	A=0.2422
Latin American 2	Sub	9346	C=0.6541	A=0.3459
South Asian	Sub	5236	C=0.6830	A=0.3170
Other	Sub	10506	C=0.75966	A=0.24034

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	311400	C=0.751317	A=0.248683
Allele Frequency Aggregator	European	Sub	272786	C=0.752234	A=0.247766
Allele Frequency Aggregator	Other	Sub	9706	C=0.7607	A=0.2393
Allele Frequency Aggregator	Latin American 2	Sub	9346	C=0.6541	A=0.3459
Allele Frequency Aggregator	African	Sub	9062	C=0.8792	A=0.1208
Allele Frequency Aggregator	South Asian	Sub	5236	C=0.6830	A=0.3170
Allele Frequency Aggregator	Asian	Sub	3988	C=0.6908	A=0.3092
Allele Frequency Aggregator	Latin American 1	Sub	1276	C=0.7578	A=0.2422
TopMed	Global	Study-wide	264690	C=0.781238	A=0.218762
gnomAD - Genomes	Global	Study-wide	139890	C=0.782450	A=0.217550
gnomAD - Genomes	European	Sub	75780	C=0.74663	A=0.25337
gnomAD - Genomes	African	Sub	41928	C=0.88137	A=0.11863
gnomAD - Genomes	American	Sub	13592	C=0.71292	A=0.28708
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	C=0.7194	A=0.2806
gnomAD - Genomes	East Asian	Sub	3128	C=0.7081	A=0.2919
gnomAD - Genomes	Other	Sub	2140	C=0.7607	A=0.2393
The PAGE Study	Global	Study-wide	78700	C=0.78220	A=0.21780
The PAGE Study	AfricanAmerican	Sub	32516	C=0.87788	A=0.12212
The PAGE Study	Mexican	Sub	10810	C=0.65051	A=0.34949
The PAGE Study	Asian	Sub	8316	C=0.6645	A=0.3355
The PAGE Study	PuertoRican	Sub	7918	C=0.7259	A=0.2741
The PAGE Study	NativeHawaiian	Sub	4534	C=0.8216	A=0.1784
The PAGE Study	Cuban	Sub	4230	C=0.7688	A=0.2312
The PAGE Study	Dominican	Sub	3828	C=0.8229	A=0.1771
The PAGE Study	CentralAmerican	Sub	2450	C=0.6849	A=0.3151
The PAGE Study	SouthAmerican	Sub	1982	C=0.7033	A=0.2967
The PAGE Study	NativeAmerican	Sub	1260	C=0.7214	A=0.2786
The PAGE Study	SouthAsian	Sub	856	C=0.701	A=0.299
14KJPN	JAPANESE	Study-wide	28256	C=0.64648	A=0.35352
8.3KJPN	JAPANESE	Study-wide	16760	C=0.64445	A=0.35555
1000Genomes_30x	Global	Study-wide	6404	C=0.7751	A=0.2249
1000Genomes_30x	African	Sub	1786	C=0.9031	A=0.0969
1000Genomes_30x	Europe	Sub	1266	C=0.7536	A=0.2464
1000Genomes_30x	South Asian	Sub	1202	C=0.7188	A=0.2812
1000Genomes_30x	East Asian	Sub	1170	C=0.7145	A=0.2855
1000Genomes_30x	American	Sub	980	C=0.711	A=0.289
1000Genomes	Global	Study-wide	5008	C=0.7688	A=0.2312
1000Genomes	African	Sub	1322	C=0.9024	A=0.0976
1000Genomes	East Asian	Sub	1008	C=0.7093	A=0.2907
1000Genomes	Europe	Sub	1006	C=0.7465	A=0.2535
1000Genomes	South Asian	Sub	978	C=0.721	A=0.279
1000Genomes	American	Sub	694	C=0.700	A=0.300
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.7176	A=0.2824
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.7571	A=0.2429
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.7611	A=0.2389
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.6465	A=0.3535
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.6852	A=0.3148
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.623	A=0.377
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.650	A=0.350
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.794	A=0.206
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.756	A=0.244
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.764	A=0.236
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.440	A=0.560
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.92	A=0.08
HapMap	Global	Study-wide	1892	C=0.7828	A=0.2172
HapMap	American	Sub	770	C=0.727	A=0.273
HapMap	African	Sub	692	C=0.884	A=0.116
HapMap	Asian	Sub	254	C=0.717	A=0.283
HapMap	Europe	Sub	176	C=0.722	A=0.278
Korean Genome Project	KOREAN	Study-wide	1832	C=0.6337	A=0.3663
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.729	A=0.271
CNV burdens in cranial meningiomas	Global	Study-wide	788	C=0.678	A=0.322
CNV burdens in cranial meningiomas	CRM	Sub	788	C=0.678	A=0.322
Chileans	Chilean	Study-wide	626	C=0.674	A=0.326
Northern Sweden	ACPOP	Study-wide	600	C=0.703	A=0.297
SGDP_PRJ	Global	Study-wide	242	C=0.393	A=0.607
Qatari	Global	Study-wide	216	C=0.819	A=0.181
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.722	A=0.278
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	86	C=0.86	A=0.14
The Danish reference pan genome	Danish	Study-wide	40	C=0.82	A=0.17
Siberian	Global	Study-wide	38	C=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 1	NC_000001.11:g.218535261C>A
GRCh37.p13 chr 1	NC_000001.10:g.218708603C>A

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	C=	A
GRCh38.p14 chr 1	NC_000001.11:g.218535261=	NC_000001.11:g.218535261C>A
GRCh37.p13 chr 1	NC_000001.10:g.218708603=	NC_000001.10:g.218708603C>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#.

132 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2957220	Apr 12, 2001 (94)
2	PERLEGEN	ss24261029	Sep 20, 2004 (123)
3	ABI	ss43960174	Mar 15, 2006 (126)
4	AFFY	ss66298895	Dec 02, 2006 (127)
5	ILLUMINA	ss66642864	Dec 02, 2006 (127)
6	ILLUMINA	ss67219057	Dec 02, 2006 (127)
7	ILLUMINA	ss67613135	Dec 02, 2006 (127)
8	ILLUMINA	ss70697337	May 24, 2008 (130)
9	ILLUMINA	ss71263020	May 18, 2007 (127)
10	ILLUMINA	ss75533346	Dec 07, 2007 (129)
11	AFFY	ss75969192	Dec 07, 2007 (129)
12	HGSV	ss78447477	Dec 07, 2007 (129)
13	ILLUMINA	ss79110120	Dec 15, 2007 (130)
14	KRIBB_YJKIM	ss83955520	Dec 15, 2007 (130)
15	BCMHGSC_JDW	ss87974280	Mar 23, 2008 (129)
16	BGI	ss102822433	Dec 01, 2009 (131)
17	1000GENOMES	ss108957297	Jan 23, 2009 (130)
18	ILLUMINA	ss121899309	Dec 01, 2009 (131)
19	ILLUMINA	ss153831030	Dec 01, 2009 (131)
20	GMI	ss156298563	Dec 01, 2009 (131)
21	ILLUMINA	ss159352794	Dec 01, 2009 (131)
22	ILLUMINA	ss160493804	Dec 01, 2009 (131)
23	AFFY	ss169815467	Jul 04, 2010 (132)
24	ILLUMINA	ss170974510	Jul 04, 2010 (132)
25	ILLUMINA	ss173068747	Jul 04, 2010 (132)
26	1000GENOMES	ss210743078	Jul 14, 2010 (132)
27	1000GENOMES	ss218889108	Jul 14, 2010 (132)
28	1000GENOMES	ss230907461	Jul 14, 2010 (132)
29	1000GENOMES	ss238518291	Jul 15, 2010 (132)
30	BL	ss253832417	May 09, 2011 (134)
31	GMI	ss276221195	May 04, 2012 (137)
32	GMI	ss284230882	Apr 25, 2013 (138)
33	PJP	ss290736530	May 09, 2011 (134)
34	ILLUMINA	ss480397006	May 04, 2012 (137)
35	ILLUMINA	ss480410102	May 04, 2012 (137)
36	ILLUMINA	ss481189833	Sep 08, 2015 (146)
37	ILLUMINA	ss484996122	May 04, 2012 (137)
38	ILLUMINA	ss537028938	Sep 08, 2015 (146)
39	TISHKOFF	ss555147395	Apr 25, 2013 (138)
40	SSMP	ss648709641	Apr 25, 2013 (138)
41	ILLUMINA	ss779054934	Sep 08, 2015 (146)
42	ILLUMINA	ss782944362	Sep 08, 2015 (146)
43	ILLUMINA	ss783906867	Sep 08, 2015 (146)
44	ILLUMINA	ss825440638	Apr 01, 2015 (144)
45	ILLUMINA	ss832200101	Sep 08, 2015 (146)
46	ILLUMINA	ss832864722	Jul 12, 2019 (153)
47	ILLUMINA	ss834517963	Sep 08, 2015 (146)
48	EVA-GONL	ss976158253	Aug 21, 2014 (142)
49	JMKIDD_LAB	ss1068612044	Aug 21, 2014 (142)
50	1000GENOMES	ss1294700299	Aug 21, 2014 (142)
51	DDI	ss1426115615	Apr 01, 2015 (144)
52	EVA_GENOME_DK	ss1574688165	Apr 01, 2015 (144)
53	EVA_DECODE	ss1585554699	Apr 01, 2015 (144)
54	EVA_UK10K_ALSPAC	ss1602167458	Apr 01, 2015 (144)
55	EVA_UK10K_TWINSUK	ss1645161491	Apr 01, 2015 (144)
56	EVA_SVP	ss1712406474	Apr 01, 2015 (144)
57	ILLUMINA	ss1751899252	Sep 08, 2015 (146)
58	HAMMER_LAB	ss1795746865	Sep 08, 2015 (146)
59	WEILL_CORNELL_DGM	ss1919381805	Feb 12, 2016 (147)
60	ILLUMINA	ss1946023725	Feb 12, 2016 (147)
61	ILLUMINA	ss1958358400	Feb 12, 2016 (147)
62	GENOMED	ss1966976217	Jul 19, 2016 (147)
63	JJLAB	ss2020213805	Sep 14, 2016 (149)
64	USC_VALOUEV	ss2148244893	Dec 20, 2016 (150)
65	HUMAN_LONGEVITY	ss2170193405	Dec 20, 2016 (150)
66	SYSTEMSBIOZJU	ss2624615861	Nov 08, 2017 (151)
67	ILLUMINA	ss2632631254	Nov 08, 2017 (151)
68	GRF	ss2698238647	Nov 08, 2017 (151)
69	ILLUMINA	ss2710694452	Nov 08, 2017 (151)
70	GNOMAD	ss2766350555	Nov 08, 2017 (151)
71	SWEGEN	ss2988470349	Nov 08, 2017 (151)
72	ILLUMINA	ss3021181557	Nov 08, 2017 (151)
73	BIOINF_KMB_FNS_UNIBA	ss3023866973	Nov 08, 2017 (151)
74	CSHL	ss3343917418	Nov 08, 2017 (151)
75	ILLUMINA	ss3625561628	Oct 11, 2018 (152)
76	ILLUMINA	ss3626312048	Oct 11, 2018 (152)
77	ILLUMINA	ss3630661031	Oct 11, 2018 (152)
78	ILLUMINA	ss3632926060	Oct 11, 2018 (152)
79	ILLUMINA	ss3633622117	Oct 11, 2018 (152)
80	ILLUMINA	ss3634373649	Oct 11, 2018 (152)
81	ILLUMINA	ss3635315208	Oct 11, 2018 (152)
82	ILLUMINA	ss3636052569	Oct 11, 2018 (152)
83	ILLUMINA	ss3637065744	Oct 11, 2018 (152)
84	ILLUMINA	ss3637815015	Oct 11, 2018 (152)
85	ILLUMINA	ss3638922883	Oct 11, 2018 (152)
86	ILLUMINA	ss3639460303	Oct 11, 2018 (152)
87	ILLUMINA	ss3640081002	Oct 11, 2018 (152)
88	ILLUMINA	ss3640992558	Oct 11, 2018 (152)
89	ILLUMINA	ss3641286680	Oct 11, 2018 (152)
90	ILLUMINA	ss3642821326	Oct 11, 2018 (152)
91	ILLUMINA	ss3644519734	Oct 11, 2018 (152)
92	ILLUMINA	ss3651526851	Oct 11, 2018 (152)
93	EGCUT_WGS	ss3656431808	Jul 12, 2019 (153)
94	EVA_DECODE	ss3688653994	Jul 12, 2019 (153)
95	ILLUMINA	ss3725106972	Jul 12, 2019 (153)
96	ACPOP	ss3727873544	Jul 12, 2019 (153)
97	ILLUMINA	ss3744060911	Jul 12, 2019 (153)
98	ILLUMINA	ss3744674516	Jul 12, 2019 (153)
99	EVA	ss3747350331	Jul 12, 2019 (153)
100	PAGE_CC	ss3770872979	Jul 12, 2019 (153)
101	ILLUMINA	ss3772175413	Jul 12, 2019 (153)
102	KHV_HUMAN_GENOMES	ss3800355055	Jul 12, 2019 (153)
103	EVA	ss3826650030	Apr 25, 2020 (154)
104	EVA	ss3836725448	Apr 25, 2020 (154)
105	EVA	ss3842137352	Apr 25, 2020 (154)
106	HGDP	ss3847364172	Apr 25, 2020 (154)
107	SGDP_PRJ	ss3850923098	Apr 25, 2020 (154)
108	KRGDB	ss3896239460	Apr 25, 2020 (154)
109	KOGIC	ss3946515006	Apr 25, 2020 (154)
110	EVA	ss3984472215	Apr 25, 2021 (155)
111	EVA	ss3984852916	Apr 25, 2021 (155)
112	EVA	ss4016963045	Apr 25, 2021 (155)
113	TOPMED	ss4484005799	Apr 25, 2021 (155)
114	TOMMO_GENOMICS	ss5148484391	Apr 25, 2021 (155)
115	1000G_HIGH_COVERAGE	ss5245839239	Oct 12, 2022 (156)
116	EVA	ss5314683556	Oct 12, 2022 (156)
117	EVA	ss5324872207	Oct 12, 2022 (156)
118	HUGCELL_USP	ss5446274137	Oct 12, 2022 (156)
119	EVA	ss5506191041	Oct 12, 2022 (156)
120	1000G_HIGH_COVERAGE	ss5519960249	Oct 12, 2022 (156)
121	SANFORD_IMAGENETICS	ss5624230285	Oct 12, 2022 (156)
122	SANFORD_IMAGENETICS	ss5627473583	Oct 12, 2022 (156)
123	TOMMO_GENOMICS	ss5676260147	Oct 12, 2022 (156)
124	EVA	ss5799512171	Oct 12, 2022 (156)
125	YY_MCH	ss5801647554	Oct 12, 2022 (156)
126	EVA	ss5833278479	Oct 12, 2022 (156)
127	EVA	ss5847174771	Oct 12, 2022 (156)
128	EVA	ss5847574610	Oct 12, 2022 (156)
129	EVA	ss5849289734	Oct 12, 2022 (156)
130	EVA	ss5912026180	Oct 12, 2022 (156)
131	EVA	ss5939312506	Oct 12, 2022 (156)
132	EVA	ss5979305396	Oct 12, 2022 (156)
133	1000Genomes	NC_000001.10 - 218708603	Oct 11, 2018 (152)
134	1000Genomes_30x	NC_000001.11 - 218535261	Oct 12, 2022 (156)
135	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 218708603	Oct 11, 2018 (152)
136	Chileans	NC_000001.10 - 218708603	Apr 25, 2020 (154)
137	Genetic variation in the Estonian population	NC_000001.10 - 218708603	Oct 11, 2018 (152)
138	The Danish reference pan genome	NC_000001.10 - 218708603	Apr 25, 2020 (154)
139	gnomAD - Genomes	NC_000001.11 - 218535261	Apr 25, 2021 (155)
140	Genome of the Netherlands Release 5	NC_000001.10 - 218708603	Apr 25, 2020 (154)
141	HGDP-CEPH-db Supplement 1	NC_000001.9 - 216775226	Apr 25, 2020 (154)
142	HapMap	NC_000001.11 - 218535261	Apr 25, 2020 (154)
143	KOREAN population from KRGDB	NC_000001.10 - 218708603	Apr 25, 2020 (154)
144	Korean Genome Project	NC_000001.11 - 218535261	Apr 25, 2020 (154)
145	Northern Sweden	NC_000001.10 - 218708603	Jul 12, 2019 (153)
146	The PAGE Study	NC_000001.11 - 218535261	Jul 12, 2019 (153)
147	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 218708603	Apr 25, 2021 (155)
148	CNV burdens in cranial meningiomas	NC_000001.10 - 218708603	Apr 25, 2021 (155)
149	Qatari	NC_000001.10 - 218708603	Apr 25, 2020 (154)
150	SGDP_PRJ	NC_000001.10 - 218708603	Apr 25, 2020 (154)
151	Siberian	NC_000001.10 - 218708603	Apr 25, 2020 (154)
152	8.3KJPN	NC_000001.10 - 218708603	Apr 25, 2021 (155)
153	14KJPN	NC_000001.11 - 218535261	Oct 12, 2022 (156)
154	TopMed	NC_000001.11 - 218535261	Apr 25, 2021 (155)
155	UK 10K study - Twins	NC_000001.10 - 218708603	Oct 11, 2018 (152)
156	A Vietnamese Genetic Variation Database	NC_000001.10 - 218708603	Jul 12, 2019 (153)
157	ALFA	NC_000001.11 - 218535261	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)
rs17502047	Oct 07, 2004 (123)
rs58365293	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss78447477, ss3638922883, ss3639460303	NC_000001.8:215096997:C:A	NC_000001.11:218535260:C:A	(self)
42064, ss66298895, ss75969192, ss87974280, ss108957297, ss169815467, ss210743078, ss253832417, ss276221195, ss284230882, ss290736530, ss480397006, ss825440638, ss1585554699, ss1712406474, ss3642821326, ss3847364172	NC_000001.9:216775225:C:A	NC_000001.11:218535260:C:A	(self)
5556628, 3069077, 33358, 2170056, 1889964, 1341236, 3416854, 1158409, 78843, 21536, 1423735, 2940078, 761247, 6453698, 3069077, 664432, ss218889108, ss230907461, ss238518291, ss480410102, ss481189833, ss484996122, ss537028938, ss555147395, ss648709641, ss779054934, ss782944362, ss783906867, ss832200101, ss832864722, ss834517963, ss976158253, ss1068612044, ss1294700299, ss1426115615, ss1574688165, ss1602167458, ss1645161491, ss1751899252, ss1795746865, ss1919381805, ss1946023725, ss1958358400, ss1966976217, ss2020213805, ss2148244893, ss2624615861, ss2632631254, ss2698238647, ss2710694452, ss2766350555, ss2988470349, ss3021181557, ss3343917418, ss3625561628, ss3626312048, ss3630661031, ss3632926060, ss3633622117, ss3634373649, ss3635315208, ss3636052569, ss3637065744, ss3637815015, ss3640081002, ss3640992558, ss3641286680, ss3644519734, ss3651526851, ss3656431808, ss3727873544, ss3744060911, ss3744674516, ss3747350331, ss3772175413, ss3826650030, ss3836725448, ss3850923098, ss3896239460, ss3984472215, ss3984852916, ss4016963045, ss5148484391, ss5314683556, ss5324872207, ss5506191041, ss5624230285, ss5627473583, ss5799512171, ss5833278479, ss5847174771, ss5847574610, ss5939312506, ss5979305396	NC_000001.10:218708602:C:A	NC_000001.11:218535260:C:A	(self)
7486184, 39929143, 271950, 2893007, 94448, 10097251, 47612134, 5749631903, ss2170193405, ss3023866973, ss3688653994, ss3725106972, ss3770872979, ss3800355055, ss3842137352, ss3946515006, ss4484005799, ss5245839239, ss5446274137, ss5519960249, ss5676260147, ss5801647554, ss5849289734, ss5912026180	NC_000001.11:218535260:C:A	NC_000001.11:218535260:C:A	(self)
ss2957220, ss24261029, ss43960174, ss66642864, ss67219057, ss67613135, ss70697337, ss71263020, ss75533346, ss79110120, ss83955520, ss102822433, ss121899309, ss153831030, ss156298563, ss159352794, ss160493804, ss170974510, ss173068747	NT_167186.1:12226381:C:A	NC_000001.11:218535260:C:A	(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 rs2047163

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs2047163