Name: rs17791096
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.

rs17791096

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:5052173 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.466525 (137845/295472, ALFA)
A=0.385251 (101972/264690, TOPMED)
A=0.464004 (95156/205076, GENOGRAPHIC) (+ 22 more)
A=0.390356 (54628/139944, GnomAD)
A=0.34325 (27011/78692, PAGE_STUDY)
A=0.36991 (10453/28258, 14KJPN)
A=0.36754 (6160/16760, 8.3KJPN)
A=0.3737 (2393/6404, 1000G_30x)
A=0.3748 (1877/5008, 1000G)
A=0.4339 (1944/4480, Estonian)
A=0.4712 (1816/3854, ALSPAC)
A=0.4730 (1754/3708, TWINSUK)
A=0.3392 (994/2930, KOREAN)
A=0.4227 (880/2082, HGDP_Stanford)
A=0.3256 (614/1886, HapMap)
A=0.3253 (596/1832, Korea1K)
A=0.485 (484/998, GoNL)
A=0.351 (278/792, PRJEB37584)
A=0.463 (278/600, NorthernSweden)
G=0.325 (123/378, SGDP_PRJ)
G=0.468 (101/216, Qatari)
A=0.361 (78/216, Vietnamese)
A=0.45 (18/40, GENOME_DK)
G=0.40 (16/40, Ancient Sardinia)
G=0.38 (12/32, 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	300506	G=0.534515	A=0.465485, C=0.000000
European	Sub	268152	G=0.524247	A=0.475753, C=0.000000
African	Sub	9258	G=0.7846	A=0.2154, C=0.0000
African Others	Sub	366	G=0.863	A=0.137, C=0.000
African American	Sub	8892	G=0.7814	A=0.2186, C=0.0000
Asian	Sub	3924	G=0.6195	A=0.3805, C=0.0000
East Asian	Sub	3178	G=0.6671	A=0.3329, C=0.0000
Other Asian	Sub	746	G=0.417	A=0.583, C=0.000
Latin American 1	Sub	1064	G=0.5874	A=0.4126, C=0.0000
Latin American 2	Sub	3158	G=0.5472	A=0.4528, C=0.0000
South Asian	Sub	5202	G=0.5315	A=0.4685, C=0.0000
Other	Sub	9748	G=0.5369	A=0.4631, C=0.0000

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	295472	G=0.533475	A=0.466525, C=0.000000
Allele Frequency Aggregator	European	Sub	265060	G=0.524134	A=0.475866, C=0.000000
Allele Frequency Aggregator	Other	Sub	8948	G=0.5353	A=0.4647, C=0.0000
Allele Frequency Aggregator	African	Sub	8116	G=0.7838	A=0.2162, C=0.0000
Allele Frequency Aggregator	South Asian	Sub	5202	G=0.5315	A=0.4685, C=0.0000
Allele Frequency Aggregator	Asian	Sub	3924	G=0.6195	A=0.3805, C=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	3158	G=0.5472	A=0.4528, C=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	1064	G=0.5874	A=0.4126, C=0.0000
TopMed	Global	Study-wide	264690	G=0.614749	A=0.385251
Genographic Project	Global	Study-wide	205076	G=0.535996	A=0.464004
gnomAD - Genomes	Global	Study-wide	139944	G=0.609644	A=0.390356
gnomAD - Genomes	European	Sub	75806	G=0.53115	A=0.46885
gnomAD - Genomes	African	Sub	41932	G=0.77511	A=0.22489
gnomAD - Genomes	American	Sub	13622	G=0.56262	A=0.43738
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	G=0.4870	A=0.5130
gnomAD - Genomes	East Asian	Sub	3120	G=0.6468	A=0.3532
gnomAD - Genomes	Other	Sub	2144	G=0.5835	A=0.4165
The PAGE Study	Global	Study-wide	78692	G=0.65675	A=0.34325
The PAGE Study	AfricanAmerican	Sub	32514	G=0.77610	A=0.22390
The PAGE Study	Mexican	Sub	10806	G=0.55182	A=0.44818
The PAGE Study	Asian	Sub	8318	G=0.6301	A=0.3699
The PAGE Study	PuertoRican	Sub	7918	G=0.5808	A=0.4192
The PAGE Study	NativeHawaiian	Sub	4534	G=0.4665	A=0.5335
The PAGE Study	Cuban	Sub	4228	G=0.5409	A=0.4591
The PAGE Study	Dominican	Sub	3828	G=0.6382	A=0.3618
The PAGE Study	CentralAmerican	Sub	2450	G=0.5886	A=0.4114
The PAGE Study	SouthAmerican	Sub	1980	G=0.5975	A=0.4025
The PAGE Study	NativeAmerican	Sub	1260	G=0.5921	A=0.4079
The PAGE Study	SouthAsian	Sub	856	G=0.500	A=0.500
14KJPN	JAPANESE	Study-wide	28258	G=0.63009	A=0.36991
8.3KJPN	JAPANESE	Study-wide	16760	G=0.63246	A=0.36754
1000Genomes_30x	Global	Study-wide	6404	G=0.6263	A=0.3737
1000Genomes_30x	African	Sub	1786	G=0.8477	A=0.1523
1000Genomes_30x	Europe	Sub	1266	G=0.4905	A=0.5095
1000Genomes_30x	South Asian	Sub	1202	G=0.4933	A=0.5067
1000Genomes_30x	East Asian	Sub	1170	G=0.6615	A=0.3385
1000Genomes_30x	American	Sub	980	G=0.519	A=0.481
1000Genomes	Global	Study-wide	5008	G=0.6252	A=0.3748
1000Genomes	African	Sub	1322	G=0.8404	A=0.1596
1000Genomes	East Asian	Sub	1008	G=0.6647	A=0.3353
1000Genomes	Europe	Sub	1006	G=0.5070	A=0.4930
1000Genomes	South Asian	Sub	978	G=0.487	A=0.513
1000Genomes	American	Sub	694	G=0.524	A=0.476
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.5661	A=0.4339
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.5288	A=0.4712
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.5270	A=0.4730
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.6608	A=0.3392
HGDP-CEPH-db Supplement 1	Global	Study-wide	2082	G=0.5773	A=0.4227
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	G=0.617	A=0.383
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	G=0.560	A=0.440
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.577	A=0.423
HGDP-CEPH-db Supplement 1	Europe	Sub	318	G=0.475	A=0.525
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.793	A=0.207
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.593	A=0.407
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.10	A=0.90
HapMap	Global	Study-wide	1886	G=0.6744	A=0.3256
HapMap	American	Sub	768	G=0.591	A=0.409
HapMap	African	Sub	688	G=0.820	A=0.180
HapMap	Asian	Sub	254	G=0.669	A=0.331
HapMap	Europe	Sub	176	G=0.477	A=0.523
Korean Genome Project	KOREAN	Study-wide	1832	G=0.6747	A=0.3253
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.515	A=0.485
CNV burdens in cranial meningiomas	Global	Study-wide	792	G=0.649	A=0.351
CNV burdens in cranial meningiomas	CRM	Sub	792	G=0.649	A=0.351
Northern Sweden	ACPOP	Study-wide	600	G=0.537	A=0.463
SGDP_PRJ	Global	Study-wide	378	G=0.325	A=0.675
Qatari	Global	Study-wide	216	G=0.468	A=0.532
A Vietnamese Genetic Variation Database	Global	Study-wide	216	G=0.639	A=0.361
The Danish reference pan genome	Danish	Study-wide	40	G=0.55	A=0.45
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	40	G=0.40	A=0.60
Siberian	Global	Study-wide	32	G=0.38	A=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 3	NC_000003.12:g.5052173G>A
GRCh38.p14 chr 3	NC_000003.12:g.5052173G>C
GRCh37.p13 chr 3	NC_000003.11:g.5093858G>A
GRCh37.p13 chr 3	NC_000003.11:g.5093858G>C

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
GRCh38.p14 chr 3	NC_000003.12:g.5052173=	NC_000003.12:g.5052173G>A	NC_000003.12:g.5052173G>C
GRCh37.p13 chr 3	NC_000003.11:g.5093858=	NC_000003.11:g.5093858G>A	NC_000003.11:g.5093858G>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#.

133 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss24298814	Sep 20, 2004 (123)
2	ABI	ss28532863	Dec 02, 2004 (126)
3	ILLUMINA	ss67194565	Nov 30, 2006 (127)
4	ILLUMINA	ss67580344	Nov 30, 2006 (127)
5	ILLUMINA	ss68187426	Dec 12, 2006 (127)
6	ILLUMINA	ss70672756	May 25, 2008 (130)
7	ILLUMINA	ss71235395	May 17, 2007 (127)
8	ILLUMINA	ss75483314	Dec 07, 2007 (129)
9	HGSV	ss85332435	Dec 15, 2007 (130)
10	KRIBB_YJKIM	ss85405734	Dec 15, 2007 (130)
11	BCMHGSC_JDW	ss91979041	Mar 24, 2008 (129)
12	HUMANGENOME_JCVI	ss95980771	Feb 05, 2009 (130)
13	1000GENOMES	ss111163700	Jan 25, 2009 (130)
14	ILLUMINA-UK	ss116953910	Feb 14, 2009 (130)
15	ILLUMINA	ss153722884	Dec 01, 2009 (131)
16	ILLUMINA	ss159327115	Dec 01, 2009 (131)
17	ILLUMINA	ss160457877	Dec 01, 2009 (131)
18	COMPLETE_GENOMICS	ss161902695	Jul 04, 2010 (132)
19	ILLUMINA	ss172899553	Jul 04, 2010 (132)
20	BUSHMAN	ss202061848	Jul 04, 2010 (132)
21	1000GENOMES	ss219950525	Jul 14, 2010 (132)
22	1000GENOMES	ss231685789	Jul 14, 2010 (132)
23	1000GENOMES	ss239123848	Jul 15, 2010 (132)
24	BL	ss252898499	May 09, 2011 (134)
25	GMI	ss276992009	May 04, 2012 (137)
26	GMI	ss284584497	Apr 25, 2013 (138)
27	PJP	ss292851799	May 09, 2011 (134)
28	ILLUMINA	ss480285624	May 04, 2012 (137)
29	ILLUMINA	ss480296798	May 04, 2012 (137)
30	ILLUMINA	ss481047299	Sep 08, 2015 (146)
31	ILLUMINA	ss484940743	May 04, 2012 (137)
32	ILLUMINA	ss536986125	Sep 08, 2015 (146)
33	TISHKOFF	ss556389035	Apr 25, 2013 (138)
34	SSMP	ss650052765	Apr 25, 2013 (138)
35	ILLUMINA	ss778466218	Sep 08, 2015 (146)
36	ILLUMINA	ss782916667	Sep 08, 2015 (146)
37	ILLUMINA	ss783879809	Sep 08, 2015 (146)
38	ILLUMINA	ss832171724	Sep 08, 2015 (146)
39	ILLUMINA	ss832839129	Jul 13, 2019 (153)
40	ILLUMINA	ss833921957	Sep 08, 2015 (146)
41	EVA-GONL	ss978215636	Aug 21, 2014 (142)
42	JMKIDD_LAB	ss1070131713	Aug 21, 2014 (142)
43	1000GENOMES	ss1302594163	Aug 21, 2014 (142)
44	DDI	ss1429313095	Apr 01, 2015 (144)
45	EVA_GENOME_DK	ss1579822100	Apr 01, 2015 (144)
46	EVA_DECODE	ss1587675474	Apr 01, 2015 (144)
47	EVA_UK10K_ALSPAC	ss1606303377	Apr 01, 2015 (144)
48	EVA_UK10K_TWINSUK	ss1649297410	Apr 01, 2015 (144)
49	EVA_SVP	ss1712549219	Apr 01, 2015 (144)
50	ILLUMINA	ss1752474110	Sep 08, 2015 (146)
51	HAMMER_LAB	ss1798772154	Sep 08, 2015 (146)
52	WEILL_CORNELL_DGM	ss1921467748	Feb 12, 2016 (147)
53	ILLUMINA	ss1946073217	Feb 12, 2016 (147)
54	ILLUMINA	ss1958531302	Feb 12, 2016 (147)
55	GENOMED	ss1969309553	Jul 19, 2016 (147)
56	JJLAB	ss2021285064	Sep 14, 2016 (149)
57	ILLUMINA	ss2095124940	Dec 20, 2016 (150)
58	USC_VALOUEV	ss2149352622	Dec 20, 2016 (150)
59	HUMAN_LONGEVITY	ss2248664213	Dec 20, 2016 (150)
60	SYSTEMSBIOZJU	ss2625142479	Nov 08, 2017 (151)
61	ILLUMINA	ss2633903749	Nov 08, 2017 (151)
62	GRF	ss2704709589	Nov 08, 2017 (151)
63	ILLUMINA	ss2710963786	Nov 08, 2017 (151)
64	GNOMAD	ss2788966143	Nov 08, 2017 (151)
65	SWEGEN	ss2991747192	Nov 08, 2017 (151)
66	ILLUMINA	ss3022205739	Nov 08, 2017 (151)
67	BIOINF_KMB_FNS_UNIBA	ss3024404619	Nov 08, 2017 (151)
68	CSHL	ss3344858789	Nov 08, 2017 (151)
69	ILLUMINA	ss3625806882	Oct 11, 2018 (152)
70	ILLUMINA	ss3628577045	Oct 11, 2018 (152)
71	ILLUMINA	ss3631852788	Oct 11, 2018 (152)
72	ILLUMINA	ss3633279767	Oct 11, 2018 (152)
73	ILLUMINA	ss3633996132	Oct 11, 2018 (152)
74	ILLUMINA	ss3634877485	Oct 11, 2018 (152)
75	ILLUMINA	ss3635680389	Oct 11, 2018 (152)
76	ILLUMINA	ss3636573451	Oct 11, 2018 (152)
77	ILLUMINA	ss3637432677	Oct 11, 2018 (152)
78	ILLUMINA	ss3638393892	Oct 11, 2018 (152)
79	ILLUMINA	ss3639200594	Oct 11, 2018 (152)
80	ILLUMINA	ss3639901563	Oct 11, 2018 (152)
81	ILLUMINA	ss3640584788	Oct 11, 2018 (152)
82	ILLUMINA	ss3641141147	Oct 11, 2018 (152)
83	ILLUMINA	ss3641437649	Oct 11, 2018 (152)
84	ILLUMINA	ss3643352546	Oct 11, 2018 (152)
85	ILLUMINA	ss3643948698	Oct 11, 2018 (152)
86	ILLUMINA	ss3644805745	Oct 11, 2018 (152)
87	URBANLAB	ss3647329665	Oct 11, 2018 (152)
88	ILLUMINA	ss3652671433	Oct 11, 2018 (152)
89	EGCUT_WGS	ss3659644646	Jul 13, 2019 (153)
90	EVA_DECODE	ss3708535586	Jul 13, 2019 (153)
91	ILLUMINA	ss3725984936	Jul 13, 2019 (153)
92	ACPOP	ss3729586112	Jul 13, 2019 (153)
93	ILLUMINA	ss3744209544	Jul 13, 2019 (153)
94	ILLUMINA	ss3745177301	Jul 13, 2019 (153)
95	EVA	ss3759594755	Jul 13, 2019 (153)
96	PAGE_CC	ss3771006323	Jul 13, 2019 (153)
97	ILLUMINA	ss3772673108	Jul 13, 2019 (153)
98	PACBIO	ss3784220619	Jul 13, 2019 (153)
99	PACBIO	ss3789751123	Jul 13, 2019 (153)
100	PACBIO	ss3794624853	Jul 13, 2019 (153)
101	KHV_HUMAN_GENOMES	ss3802745522	Jul 13, 2019 (153)
102	EVA	ss3827633672	Apr 25, 2020 (154)
103	EVA	ss3837238166	Apr 25, 2020 (154)
104	EVA	ss3842661743	Apr 25, 2020 (154)
105	HGDP	ss3847695804	Apr 25, 2020 (154)
106	SGDP_PRJ	ss3855114890	Apr 25, 2020 (154)
107	KRGDB	ss3900880751	Apr 25, 2020 (154)
108	KOGIC	ss3950564994	Apr 25, 2020 (154)
109	EVA	ss3984502020	Apr 27, 2021 (155)
110	EVA	ss3984969348	Apr 27, 2021 (155)
111	EVA	ss4017061919	Apr 27, 2021 (155)
112	TOPMED	ss4552518919	Apr 27, 2021 (155)
113	TOMMO_GENOMICS	ss5157571641	Apr 27, 2021 (155)
114	EVA	ss5237317102	Apr 27, 2021 (155)
115	1000G_HIGH_COVERAGE	ss5252867653	Oct 12, 2022 (156)
116	GENOGRAPHIC	ss5314488123	Oct 12, 2022 (156)
117	EVA	ss5314828716	Oct 12, 2022 (156)
118	EVA	ss5337559734	Oct 12, 2022 (156)
119	HUGCELL_USP	ss5452389741	Oct 12, 2022 (156)
120	EVA	ss5506868468	Oct 12, 2022 (156)
121	1000G_HIGH_COVERAGE	ss5530611391	Oct 12, 2022 (156)
122	SANFORD_IMAGENETICS	ss5624508339	Oct 12, 2022 (156)
123	SANFORD_IMAGENETICS	ss5631436424	Oct 12, 2022 (156)
124	TOMMO_GENOMICS	ss5688775565	Oct 12, 2022 (156)
125	EVA	ss5799567719	Oct 12, 2022 (156)
126	YY_MCH	ss5803434567	Oct 12, 2022 (156)
127	EVA	ss5825274865	Oct 12, 2022 (156)
128	EVA	ss5847210836	Oct 12, 2022 (156)
129	EVA	ss5847951736	Oct 12, 2022 (156)
130	EVA	ss5853466554	Oct 12, 2022 (156)
131	EVA	ss5867422362	Oct 12, 2022 (156)
132	EVA	ss5959693115	Oct 12, 2022 (156)
133	EVA	ss5979643788	Oct 12, 2022 (156)
134	1000Genomes	NC_000003.11 - 5093858	Oct 11, 2018 (152)
135	1000Genomes_30x	NC_000003.12 - 5052173	Oct 12, 2022 (156)
136	The Avon Longitudinal Study of Parents and Children	NC_000003.11 - 5093858	Oct 11, 2018 (152)
137	Genetic variation in the Estonian population	NC_000003.11 - 5093858	Oct 11, 2018 (152)
138	Genographic Project	NC_000003.12 - 5052173	Oct 12, 2022 (156)
139	The Danish reference pan genome	NC_000003.11 - 5093858	Apr 25, 2020 (154)
140	gnomAD - Genomes	NC_000003.12 - 5052173	Apr 27, 2021 (155)
141	Genome of the Netherlands Release 5	NC_000003.11 - 5093858	Apr 25, 2020 (154)
142	HGDP-CEPH-db Supplement 1	NC_000003.10 - 5068858	Apr 25, 2020 (154)
143	HapMap	NC_000003.12 - 5052173	Apr 25, 2020 (154)
144	KOREAN population from KRGDB	NC_000003.11 - 5093858	Apr 25, 2020 (154)
145	Korean Genome Project	NC_000003.12 - 5052173	Apr 25, 2020 (154)
146	Northern Sweden	NC_000003.11 - 5093858	Jul 13, 2019 (153)
147	The PAGE Study	NC_000003.12 - 5052173	Jul 13, 2019 (153)
148	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000003.11 - 5093858	Apr 27, 2021 (155)
149	CNV burdens in cranial meningiomas	NC_000003.11 - 5093858	Apr 27, 2021 (155)
150	Qatari	NC_000003.11 - 5093858	Apr 25, 2020 (154)
151	SGDP_PRJ	NC_000003.11 - 5093858	Apr 25, 2020 (154)
152	Siberian	NC_000003.11 - 5093858	Apr 25, 2020 (154)
153	8.3KJPN	NC_000003.11 - 5093858	Apr 27, 2021 (155)
154	14KJPN	NC_000003.12 - 5052173	Oct 12, 2022 (156)
155	TopMed	NC_000003.12 - 5052173	Apr 27, 2021 (155)
156	UK 10K study - Twins	NC_000003.11 - 5093858	Oct 11, 2018 (152)
157	A Vietnamese Genetic Variation Database	NC_000003.11 - 5093858	Jul 13, 2019 (153)
158	ALFA	NC_000003.12 - 5052173	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)
rs17885197	May 23, 2006 (127)
rs59648716	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss85332435, ss3639200594, ss3639901563, ss3643948698	NC_000003.9:5068857:G:A	NC_000003.12:5052172:G:A	(self)
373696, ss91979041, ss111163700, ss116953910, ss161902695, ss202061848, ss252898499, ss276992009, ss284584497, ss292851799, ss480285624, ss1587675474, ss1712549219, ss3643352546, ss3847695804	NC_000003.10:5068857:G:A	NC_000003.12:5052172:G:A	(self)
13732293, 7610648, 5382894, 5987039, 3339750, 8058145, 2870977, 195275, 51361, 3509678, 7131870, 1868976, 15540948, 7610648, 1655764, ss219950525, ss231685789, ss239123848, ss480296798, ss481047299, ss484940743, ss536986125, ss556389035, ss650052765, ss778466218, ss782916667, ss783879809, ss832171724, ss832839129, ss833921957, ss978215636, ss1070131713, ss1302594163, ss1429313095, ss1579822100, ss1606303377, ss1649297410, ss1752474110, ss1798772154, ss1921467748, ss1946073217, ss1958531302, ss1969309553, ss2021285064, ss2095124940, ss2149352622, ss2625142479, ss2633903749, ss2704709589, ss2710963786, ss2788966143, ss2991747192, ss3022205739, ss3344858789, ss3625806882, ss3628577045, ss3631852788, ss3633279767, ss3633996132, ss3634877485, ss3635680389, ss3636573451, ss3637432677, ss3638393892, ss3640584788, ss3641141147, ss3641437649, ss3644805745, ss3652671433, ss3659644646, ss3729586112, ss3744209544, ss3745177301, ss3759594755, ss3772673108, ss3784220619, ss3789751123, ss3794624853, ss3827633672, ss3837238166, ss3855114890, ss3900880751, ss3984502020, ss3984969348, ss4017061919, ss5157571641, ss5237317102, ss5314828716, ss5337559734, ss5506868468, ss5624508339, ss5631436424, ss5799567719, ss5825274865, ss5847210836, ss5847951736, ss5959693115, ss5979643788	NC_000003.11:5093857:G:A	NC_000003.12:5052172:G:A	(self)
18137326, 80196, 97604474, 2292061, 6942995, 227792, 22612669, 389896474, 794827078, ss2248664213, ss3024404619, ss3647329665, ss3708535586, ss3725984936, ss3771006323, ss3802745522, ss3842661743, ss3950564994, ss4552518919, ss5252867653, ss5314488123, ss5452389741, ss5530611391, ss5688775565, ss5803434567, ss5853466554, ss5867422362	NC_000003.12:5052172:G:A	NC_000003.12:5052172:G:A	(self)
ss24298814, ss28532863, ss67194565, ss67580344, ss68187426, ss70672756, ss71235395, ss75483314, ss85405734, ss95980771, ss153722884, ss159327115, ss160457877, ss172899553	NT_022517.18:5033857:G:A	NC_000003.12:5052172:G:A	(self)
794827078	NC_000003.12:5052172:G:C	NC_000003.12:5052172:G: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 rs17791096

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs17791096