Name: rs2176528
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.

rs2176528

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:194007459 (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 / C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.276278 (73128/264690, TOPMED)
G=0.27536 (21713/78854, ALFA)
G=0.31363 (24671/78664, PAGE_STUDY) (+ 18 more)
G=0.3406 (2181/6404, 1000G_30x)
G=0.3409 (1707/5008, 1000G)
G=0.2683 (1202/4480, Estonian)
G=0.2818 (1086/3854, ALSPAC)
G=0.2875 (1066/3708, TWINSUK)
C=0.3676 (1077/2930, KOREAN)
C=0.3941 (722/1832, Korea1K)
G=0.3116 (354/1136, Daghestan)
G=0.289 (288/998, GoNL)
C=0.385 (303/788, PRJEB37584)
G=0.320 (192/600, NorthernSweden)
G=0.320 (105/328, HapMap)
C=0.347 (113/326, SGDP_PRJ)
G=0.264 (57/216, Qatari)
C=0.425 (91/214, Vietnamese)
G=0.24 (16/66, Ancient Sardinia)
G=0.15 (6/40, GENOME_DK)
C=0.37 (14/38, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 2 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	78854	C=0.72464	G=0.27536, T=0.00000
European	Sub	70158	C=0.73132	G=0.26868, T=0.00000
African	Sub	3042	C=0.9573	G=0.0427, T=0.0000
African Others	Sub	150	C=0.973	G=0.027, T=0.000
African American	Sub	2892	C=0.9564	G=0.0436, T=0.0000
Asian	Sub	3170	C=0.3823	G=0.6177, T=0.0000
East Asian	Sub	2564	C=0.3869	G=0.6131, T=0.0000
Other Asian	Sub	606	C=0.363	G=0.637, T=0.000
Latin American 1	Sub	358	C=0.799	G=0.201, T=0.000
Latin American 2	Sub	490	C=0.716	G=0.284, T=0.000
South Asian	Sub	210	C=0.676	G=0.324, T=0.000
Other	Sub	1426	C=0.6522	G=0.3478, T=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
TopMed	Global	Study-wide	264690	C=0.723722	G=0.276278
Allele Frequency Aggregator	Total	Global	78854	C=0.72464	G=0.27536, T=0.00000
Allele Frequency Aggregator	European	Sub	70158	C=0.73132	G=0.26868, T=0.00000
Allele Frequency Aggregator	Asian	Sub	3170	C=0.3823	G=0.6177, T=0.0000
Allele Frequency Aggregator	African	Sub	3042	C=0.9573	G=0.0427, T=0.0000
Allele Frequency Aggregator	Other	Sub	1426	C=0.6522	G=0.3478, T=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	490	C=0.716	G=0.284, T=0.000
Allele Frequency Aggregator	Latin American 1	Sub	358	C=0.799	G=0.201, T=0.000
Allele Frequency Aggregator	South Asian	Sub	210	C=0.676	G=0.324, T=0.000
The PAGE Study	Global	Study-wide	78664	C=0.68637	G=0.31363
The PAGE Study	AfricanAmerican	Sub	32504	C=0.86085	G=0.13915
The PAGE Study	Mexican	Sub	10802	C=0.55397	G=0.44603
The PAGE Study	Asian	Sub	8308	C=0.3993	G=0.6007
The PAGE Study	PuertoRican	Sub	7918	C=0.7070	G=0.2930
The PAGE Study	NativeHawaiian	Sub	4534	C=0.3509	G=0.6491
The PAGE Study	Cuban	Sub	4226	C=0.6829	G=0.3171
The PAGE Study	Dominican	Sub	3826	C=0.7669	G=0.2331
The PAGE Study	CentralAmerican	Sub	2450	C=0.5335	G=0.4665
The PAGE Study	SouthAmerican	Sub	1980	C=0.5172	G=0.4828
The PAGE Study	NativeAmerican	Sub	1260	C=0.6825	G=0.3175
The PAGE Study	SouthAsian	Sub	856	C=0.597	G=0.403
1000Genomes_30x	Global	Study-wide	6404	C=0.6594	G=0.3406
1000Genomes_30x	African	Sub	1786	C=0.9104	G=0.0896
1000Genomes_30x	Europe	Sub	1266	C=0.7306	G=0.2694
1000Genomes_30x	South Asian	Sub	1202	C=0.5840	G=0.4160
1000Genomes_30x	East Asian	Sub	1170	C=0.3744	G=0.6256
1000Genomes_30x	American	Sub	980	C=0.543	G=0.457
1000Genomes	Global	Study-wide	5008	C=0.6591	G=0.3409
1000Genomes	African	Sub	1322	C=0.9160	G=0.0840
1000Genomes	East Asian	Sub	1008	C=0.3700	G=0.6300
1000Genomes	Europe	Sub	1006	C=0.7386	G=0.2614
1000Genomes	South Asian	Sub	978	C=0.599	G=0.401
1000Genomes	American	Sub	694	C=0.559	G=0.441
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.7317	G=0.2683
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.7182	G=0.2818
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.7125	G=0.2875
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.3676	G=0.6324, T=0.0000
Korean Genome Project	KOREAN	Study-wide	1832	C=0.3941	G=0.6059
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	C=0.6884	G=0.3116
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	C=0.702	G=0.298
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	C=0.681	G=0.319
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.615	G=0.385
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.713	G=0.287
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	C=0.60	G=0.40
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.89	G=0.11
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.711	G=0.289
CNV burdens in cranial meningiomas	Global	Study-wide	788	C=0.385	G=0.615
CNV burdens in cranial meningiomas	CRM	Sub	788	C=0.385	G=0.615
Northern Sweden	ACPOP	Study-wide	600	C=0.680	G=0.320
HapMap	Global	Study-wide	328	C=0.680	G=0.320
HapMap	African	Sub	120	C=0.933	G=0.067
HapMap	American	Sub	120	C=0.617	G=0.383
HapMap	Asian	Sub	88	C=0.42	G=0.58
SGDP_PRJ	Global	Study-wide	326	C=0.347	G=0.653
Qatari	Global	Study-wide	216	C=0.736	G=0.264
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.425	G=0.575
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	66	C=0.76	G=0.24
The Danish reference pan genome	Danish	Study-wide	40	C=0.85	G=0.15
Siberian	Global	Study-wide	38	C=0.37	G=0.63

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 2	NC_000002.12:g.194007459C>A
GRCh38.p14 chr 2	NC_000002.12:g.194007459C>G
GRCh38.p14 chr 2	NC_000002.12:g.194007459C>T
GRCh37.p13 chr 2	NC_000002.11:g.194872183C>A
GRCh37.p13 chr 2	NC_000002.11:g.194872183C>G
GRCh37.p13 chr 2	NC_000002.11:g.194872183C>T

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	G	T
GRCh38.p14 chr 2	NC_000002.12:g.194007459=	NC_000002.12:g.194007459C>A	NC_000002.12:g.194007459C>G	NC_000002.12:g.194007459C>T
GRCh37.p13 chr 2	NC_000002.11:g.194872183=	NC_000002.11:g.194872183C>A	NC_000002.11:g.194872183C>G	NC_000002.11:g.194872183C>T

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#.

89 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss3112411	Jun 15, 2001 (96)
2	PERLEGEN	ss24170196	Sep 20, 2004 (123)
3	PERLEGEN	ss68839128	May 16, 2007 (127)
4	BGI	ss103652321	Dec 01, 2009 (131)
5	1000GENOMES	ss110514274	Jan 24, 2009 (130)
6	GMI	ss158139818	Dec 01, 2009 (131)
7	COMPLETE_GENOMICS	ss165785112	Jul 04, 2010 (132)
8	BCM-HGSC-SUB	ss205711165	Jul 04, 2010 (132)
9	1000GENOMES	ss219733089	Jul 14, 2010 (132)
10	1000GENOMES	ss231529155	Jul 14, 2010 (132)
11	1000GENOMES	ss239003920	Jul 15, 2010 (132)
12	GMI	ss276845255	May 04, 2012 (137)
13	ILLUMINA	ss483506634	May 04, 2012 (137)
14	ILLUMINA	ss483983967	May 04, 2012 (137)
15	ILLUMINA	ss535714643	Sep 08, 2015 (146)
16	TISHKOFF	ss556127036	Apr 25, 2013 (138)
17	SSMP	ss649790907	Apr 25, 2013 (138)
18	ILLUMINA	ss780303198	Aug 21, 2014 (142)
19	ILLUMINA	ss782196724	Aug 21, 2014 (142)
20	ILLUMINA	ss835789964	Aug 21, 2014 (142)
21	EVA-GONL	ss977802160	Aug 21, 2014 (142)
22	JMKIDD_LAB	ss1069823349	Aug 21, 2014 (142)
23	1000GENOMES	ss1301032857	Aug 21, 2014 (142)
24	HAMMER_LAB	ss1397316114	Sep 08, 2015 (146)
25	DDI	ss1428865595	Apr 01, 2015 (144)
26	EVA_GENOME_DK	ss1579261524	Apr 01, 2015 (144)
27	EVA_DECODE	ss1587250322	Apr 01, 2015 (144)
28	EVA_UK10K_ALSPAC	ss1605468838	Apr 01, 2015 (144)
29	EVA_UK10K_TWINSUK	ss1648462871	Apr 01, 2015 (144)
30	WEILL_CORNELL_DGM	ss1921050282	Feb 12, 2016 (147)
31	ILLUMINA	ss1946062335	Feb 12, 2016 (147)
32	ILLUMINA	ss1958491875	Feb 12, 2016 (147)
33	GENOMED	ss1968988809	Jul 19, 2016 (147)
34	JJLAB	ss2021066227	Sep 14, 2016 (149)
35	USC_VALOUEV	ss2149131298	Dec 20, 2016 (150)
36	HUMAN_LONGEVITY	ss2237854968	Dec 20, 2016 (150)
37	SYSTEMSBIOZJU	ss2625036581	Nov 08, 2017 (151)
38	ILLUMINA	ss2633721833	Nov 08, 2017 (151)
39	GRF	ss2703775803	Nov 08, 2017 (151)
40	ILLUMINA	ss2710921934	Nov 08, 2017 (151)
41	GNOMAD	ss2784559891	Nov 08, 2017 (151)
42	AFFY	ss2985816836	Nov 08, 2017 (151)
43	SWEGEN	ss2991109739	Nov 08, 2017 (151)
44	ILLUMINA	ss3022054709	Nov 08, 2017 (151)
45	BIOINF_KMB_FNS_UNIBA	ss3024293773	Nov 08, 2017 (151)
46	CSHL	ss3344674618	Nov 08, 2017 (151)
47	ILLUMINA	ss3625772891	Oct 11, 2018 (152)
48	ILLUMINA	ss3628253515	Oct 11, 2018 (152)
49	ILLUMINA	ss3631682654	Oct 11, 2018 (152)
50	ILLUMINA	ss3642146849	Oct 11, 2018 (152)
51	ILLUMINA	ss3644765001	Oct 11, 2018 (152)
52	ILLUMINA	ss3652502897	Oct 11, 2018 (152)
53	EGCUT_WGS	ss3658994282	Jul 13, 2019 (153)
54	EVA_DECODE	ss3705720649	Jul 13, 2019 (153)
55	ILLUMINA	ss3725858928	Jul 13, 2019 (153)
56	ACPOP	ss3729239843	Jul 13, 2019 (153)
57	ILLUMINA	ss3744188412	Jul 13, 2019 (153)
58	ILLUMINA	ss3744485107	Jul 13, 2019 (153)
59	EVA	ss3757903113	Jul 13, 2019 (153)
60	PAGE_CC	ss3770975297	Jul 13, 2019 (153)
61	PACBIO	ss3784109362	Jul 13, 2019 (153)
62	PACBIO	ss3789654477	Jul 13, 2019 (153)
63	PACBIO	ss3794527634	Jul 13, 2019 (153)
64	KHV_HUMAN_GENOMES	ss3802261941	Jul 13, 2019 (153)
65	EVA	ss3827429124	Apr 25, 2020 (154)
66	EVA	ss3837134103	Apr 25, 2020 (154)
67	EVA	ss3842554973	Apr 25, 2020 (154)
68	SGDP_PRJ	ss3854282956	Apr 25, 2020 (154)
69	KRGDB	ss3899956812	Apr 25, 2020 (154)
70	KOGIC	ss3949785551	Apr 25, 2020 (154)
71	EVA	ss3984495726	Apr 26, 2021 (155)
72	EVA	ss3984944995	Apr 26, 2021 (155)
73	TOPMED	ss4539160629	Apr 26, 2021 (155)
74	TOMMO_GENOMICS	ss5155799795	Apr 26, 2021 (155)
75	TOMMO_GENOMICS	ss5155799796	Apr 26, 2021 (155)
76	1000G_HIGH_COVERAGE	ss5251495525	Oct 12, 2022 (156)
77	EVA	ss5314798030	Oct 12, 2022 (156)
78	EVA	ss5335055792	Oct 12, 2022 (156)
79	HUGCELL_USP	ss5451165214	Oct 12, 2022 (156)
80	1000G_HIGH_COVERAGE	ss5528565554	Oct 12, 2022 (156)
81	SANFORD_IMAGENETICS	ss5630653184	Oct 12, 2022 (156)
82	TOMMO_GENOMICS	ss5686477431	Oct 12, 2022 (156)
83	TOMMO_GENOMICS	ss5686477432	Oct 12, 2022 (156)
84	YY_MCH	ss5803096168	Oct 12, 2022 (156)
85	EVA	ss5821383523	Oct 12, 2022 (156)
86	EVA	ss5847897298	Oct 12, 2022 (156)
87	EVA	ss5852893644	Oct 12, 2022 (156)
88	EVA	ss5934090461	Oct 12, 2022 (156)
89	EVA	ss5956895503	Oct 12, 2022 (156)
90	1000Genomes	NC_000002.11 - 194872183	Oct 11, 2018 (152)
91	1000Genomes_30x	NC_000002.12 - 194007459	Oct 12, 2022 (156)
92	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 194872183	Oct 11, 2018 (152)
93	Genome-wide autozygosity in Daghestan	NC_000002.10 - 194580428	Apr 25, 2020 (154)
94	Genetic variation in the Estonian population	NC_000002.11 - 194872183	Oct 11, 2018 (152)
95	The Danish reference pan genome	NC_000002.11 - 194872183	Apr 25, 2020 (154)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 86354375 (NC_000002.12:194007458:C:G 35615/139952) Row 86354376 (NC_000002.12:194007458:C:T 1/140002)	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 86354375 (NC_000002.12:194007458:C:G 35615/139952) Row 86354376 (NC_000002.12:194007458:C:T 1/140002)	-	Apr 26, 2021 (155)
98	Genome of the Netherlands Release 5	NC_000002.11 - 194872183	Apr 25, 2020 (154)
99	HapMap	NC_000002.12 - 194007459	Apr 25, 2020 (154)
100	KOREAN population from KRGDB	NC_000002.11 - 194872183	Apr 25, 2020 (154)
101	Korean Genome Project	NC_000002.12 - 194007459	Apr 25, 2020 (154)
102	Northern Sweden	NC_000002.11 - 194872183	Jul 13, 2019 (153)
103	The PAGE Study	NC_000002.12 - 194007459	Jul 13, 2019 (153)
104	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000002.11 - 194872183	Apr 26, 2021 (155)
105	CNV burdens in cranial meningiomas	NC_000002.11 - 194872183	Apr 26, 2021 (155)
106	Qatari	NC_000002.11 - 194872183	Apr 25, 2020 (154)
107	SGDP_PRJ	NC_000002.11 - 194872183	Apr 25, 2020 (154)
108	Siberian	NC_000002.11 - 194872183	Apr 25, 2020 (154)
109	8.3KJPN Submission ignored due to conflicting rows: Row 13769102 (NC_000002.11:194872182:C:G 10207/16760) Row 13769103 (NC_000002.11:194872182:C:A 1/16760)	-	Apr 26, 2021 (155)
110	8.3KJPN Submission ignored due to conflicting rows: Row 13769102 (NC_000002.11:194872182:C:G 10207/16760) Row 13769103 (NC_000002.11:194872182:C:A 1/16760)	-	Apr 26, 2021 (155)
111	14KJPN Submission ignored due to conflicting rows: Row 20314535 (NC_000002.12:194007458:C:G 17185/28256) Row 20314536 (NC_000002.12:194007458:C:A 1/28256)	-	Oct 12, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 20314535 (NC_000002.12:194007458:C:G 17185/28256) Row 20314536 (NC_000002.12:194007458:C:A 1/28256)	-	Oct 12, 2022 (156)
113	TopMed	NC_000002.12 - 194007459	Apr 26, 2021 (155)
114	UK 10K study - Twins	NC_000002.11 - 194872183	Oct 11, 2018 (152)
115	A Vietnamese Genetic Variation Database	NC_000002.11 - 194872183	Jul 13, 2019 (153)
116	ALFA	NC_000002.12 - 194007459	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)
rs17619732	Oct 07, 2004 (123)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5155799796	NC_000002.11:194872182:C:A	NC_000002.12:194007458:C:A	(self)
ss5686477432	NC_000002.12:194007458:C:A	NC_000002.12:194007458:C:A
265942, ss110514274, ss165785112, ss205711165, ss276845255, ss483983967, ss1397316114, ss1587250322	NC_000002.10:194580427:C:G	NC_000002.12:194007458:C:G	(self)
12114348, 6692987, 4732530, 5426463, 2938642, 7134206, 2524708, 170922, 45062, 3092212, 6299936, 1647652, 6692987, 1459552, ss219733089, ss231529155, ss239003920, ss483506634, ss535714643, ss556127036, ss649790907, ss780303198, ss782196724, ss835789964, ss977802160, ss1069823349, ss1301032857, ss1428865595, ss1579261524, ss1605468838, ss1648462871, ss1921050282, ss1946062335, ss1958491875, ss1968988809, ss2021066227, ss2149131298, ss2625036581, ss2633721833, ss2703775803, ss2710921934, ss2784559891, ss2985816836, ss2991109739, ss3022054709, ss3344674618, ss3625772891, ss3628253515, ss3631682654, ss3642146849, ss3644765001, ss3652502897, ss3658994282, ss3729239843, ss3744188412, ss3744485107, ss3757903113, ss3784109362, ss3789654477, ss3794527634, ss3827429124, ss3837134103, ss3854282956, ss3899956812, ss3984495726, ss3984944995, ss5155799795, ss5314798030, ss5335055792, ss5630653184, ss5821383523, ss5847897298, ss5956895503	NC_000002.11:194872182:C:G	NC_000002.12:194007458:C:G	(self)
16091489, 1980796, 6163552, 196766, 342983508, 1274425869, ss2237854968, ss3024293773, ss3705720649, ss3725858928, ss3770975297, ss3802261941, ss3842554973, ss3949785551, ss4539160629, ss5251495525, ss5451165214, ss5528565554, ss5686477431, ss5803096168, ss5852893644, ss5934090461	NC_000002.12:194007458:C:G	NC_000002.12:194007458:C:G	(self)
ss3112411, ss24170196, ss68839128, ss103652321, ss158139818	NT_005403.17:45081600:C:G	NC_000002.12:194007458:C:G	(self)
7134206, ss3899956812	NC_000002.11:194872182:C:T	NC_000002.12:194007458:C:T	(self)
1274425869, ss2237854968	NC_000002.12:194007458:C:T	NC_000002.12:194007458:C:T	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

2 citations for rs2176528

PMID	Title	Author	Year	Journal
21926972	Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.		2011	Nature genetics
28234206	Bipolar disorder risk gene FOXO6 modulates negative symptoms in schizophrenia: a neuroimaging genetics study.	Shenker JJ et al.	2017	Journal of psychiatry & neuroscience

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

rs2176528