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dbSNP Short Genetic Variations

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.

rs2970856

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr4:23825992 (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
G=0.175556 (46468/264690, TOPMED)
G=0.179701 (25175/140094, GnomAD)
G=0.19590 (9129/46600, ALFA) (+ 18 more)
G=0.21452 (6062/28258, 14KJPN)
G=0.21175 (3549/16760, 8.3KJPN)
G=0.1558 (998/6404, 1000G_30x)
G=0.1542 (772/5008, 1000G)
G=0.1819 (815/4480, Estonian)
G=0.2216 (854/3854, ALSPAC)
G=0.2360 (875/3708, TWINSUK)
G=0.2270 (665/2930, KOREAN)
G=0.2200 (403/1832, Korea1K)
G=0.231 (231/998, GoNL)
G=0.237 (185/780, PRJEB37584)
G=0.200 (120/600, NorthernSweden)
G=0.106 (57/540, SGDP_PRJ)
G=0.203 (67/330, HapMap)
G=0.162 (35/216, Qatari)
G=0.194 (42/216, Vietnamese)
G=0.19 (10/54, Siberian)
G=0.23 (9/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
PPARGC1A : Intron Variant
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 46600 G=0.19590 A=0.80410
European Sub 32376 G=0.21556 A=0.78444
African Sub 4936 G=0.1319 A=0.8681
African Others Sub 180 G=0.100 A=0.900
African American Sub 4756 G=0.1331 A=0.8669
Asian Sub 438 G=0.183 A=0.817
East Asian Sub 372 G=0.199 A=0.801
Other Asian Sub 66 G=0.09 A=0.91
Latin American 1 Sub 570 G=0.237 A=0.763
Latin American 2 Sub 4872 G=0.1193 A=0.8807
South Asian Sub 162 G=0.142 A=0.858
Other Sub 3246 G=0.2095 A=0.7905


Help

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 G=0.175556 A=0.824444
gnomAD - Genomes Global Study-wide 140094 G=0.179701 A=0.820299
gnomAD - Genomes European Sub 75886 G=0.21519 A=0.78481
gnomAD - Genomes African Sub 41990 G=0.12705 A=0.87295
gnomAD - Genomes American Sub 13636 G=0.14330 A=0.85670
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=0.1501 A=0.8499
gnomAD - Genomes East Asian Sub 3114 G=0.2261 A=0.7739
gnomAD - Genomes Other Sub 2144 G=0.1646 A=0.8354
Allele Frequency Aggregator Total Global 46600 G=0.19590 A=0.80410
Allele Frequency Aggregator European Sub 32376 G=0.21556 A=0.78444
Allele Frequency Aggregator African Sub 4936 G=0.1319 A=0.8681
Allele Frequency Aggregator Latin American 2 Sub 4872 G=0.1193 A=0.8807
Allele Frequency Aggregator Other Sub 3246 G=0.2095 A=0.7905
Allele Frequency Aggregator Latin American 1 Sub 570 G=0.237 A=0.763
Allele Frequency Aggregator Asian Sub 438 G=0.183 A=0.817
Allele Frequency Aggregator South Asian Sub 162 G=0.142 A=0.858
14KJPN JAPANESE Study-wide 28258 G=0.21452 A=0.78548
8.3KJPN JAPANESE Study-wide 16760 G=0.21175 A=0.78825
1000Genomes_30x Global Study-wide 6404 G=0.1558 A=0.8442
1000Genomes_30x African Sub 1786 G=0.0980 A=0.9020
1000Genomes_30x Europe Sub 1266 G=0.2038 A=0.7962
1000Genomes_30x South Asian Sub 1202 G=0.1514 A=0.8486
1000Genomes_30x East Asian Sub 1170 G=0.2188 A=0.7812
1000Genomes_30x American Sub 980 G=0.130 A=0.870
1000Genomes Global Study-wide 5008 G=0.1542 A=0.8458
1000Genomes African Sub 1322 G=0.1006 A=0.8994
1000Genomes East Asian Sub 1008 G=0.2173 A=0.7827
1000Genomes Europe Sub 1006 G=0.1948 A=0.8052
1000Genomes South Asian Sub 978 G=0.144 A=0.856
1000Genomes American Sub 694 G=0.120 A=0.880
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.1819 A=0.8181
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.2216 A=0.7784
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.2360 A=0.7640
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.2270 A=0.7730, C=0.0000
Korean Genome Project KOREAN Study-wide 1832 G=0.2200 A=0.7800
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.231 A=0.769
CNV burdens in cranial meningiomas Global Study-wide 780 G=0.237 A=0.763
CNV burdens in cranial meningiomas CRM Sub 780 G=0.237 A=0.763
Northern Sweden ACPOP Study-wide 600 G=0.200 A=0.800
SGDP_PRJ Global Study-wide 540 G=0.106 A=0.894
HapMap Global Study-wide 330 G=0.203 A=0.797
HapMap African Sub 120 G=0.075 A=0.925
HapMap American Sub 120 G=0.267 A=0.733
HapMap Asian Sub 90 G=0.29 A=0.71
Qatari Global Study-wide 216 G=0.162 A=0.838
A Vietnamese Genetic Variation Database Global Study-wide 216 G=0.194 A=0.806
Siberian Global Study-wide 54 G=0.19 A=0.81
The Danish reference pan genome Danish Study-wide 40 G=0.23 A=0.78
Help

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 4 NC_000004.12:g.23825992G>A
GRCh38.p14 chr 4 NC_000004.12:g.23825992G>C
GRCh37.p13 chr 4 NC_000004.11:g.23827615G>A
GRCh37.p13 chr 4 NC_000004.11:g.23827615G>C
PPARGC1A RefSeqGene NG_028250.2:g.651984C>T
PPARGC1A RefSeqGene NG_028250.2:g.651984C>G
Gene: PPARGC1A, PPARG coactivator 1 alpha (minus strand)
Molecule type Change Amino acid[Codon] SO Term
PPARGC1A transcript variant 1 NM_001330751.2:c.773-1484…

NM_001330751.2:c.773-1484C>T

N/A Intron Variant
PPARGC1A transcript variant 3 NM_001330752.2:c.722-1484…

NM_001330752.2:c.722-1484C>T

N/A Intron Variant
PPARGC1A transcript variant 4 NM_001330753.2:c.377-1484…

NM_001330753.2:c.377-1484C>T

N/A Intron Variant
PPARGC1A transcript variant 5 NM_001354825.2:c.773-1484…

NM_001354825.2:c.773-1484C>T

N/A Intron Variant
PPARGC1A transcript variant 6 NM_001354826.2:c.377-1484…

NM_001354826.2:c.377-1484C>T

N/A Intron Variant
PPARGC1A transcript variant 7 NM_001354827.2:c.773-1484…

NM_001354827.2:c.773-1484C>T

N/A Intron Variant
PPARGC1A transcript variant 2 NM_013261.5:c.758-1484C>T N/A Intron Variant
PPARGC1A transcript variant 8 NM_001354828.2:c. N/A Genic Downstream Transcript Variant
PPARGC1A transcript variant 9 NR_148981.2:n. N/A Intron Variant
PPARGC1A transcript variant 10 NR_148982.2:n. N/A Intron Variant
PPARGC1A transcript variant 11 NR_148983.2:n. N/A Intron Variant
PPARGC1A transcript variant 12 NR_148984.2:n. N/A Intron Variant
PPARGC1A transcript variant 13 NR_148985.2:n. N/A Intron Variant
PPARGC1A transcript variant 14 NR_148986.2:n. N/A Intron Variant
PPARGC1A transcript variant 15 NR_148987.2:n. N/A Intron Variant
PPARGC1A transcript variant X1 XM_005248131.6:c.770-1484…

XM_005248131.6:c.770-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X2 XM_005248132.1:c.749-1484…

XM_005248132.1:c.749-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X9 XM_005248134.5:c.773-1484…

XM_005248134.5:c.773-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X5 XM_011513768.2:c.653-1484…

XM_011513768.2:c.653-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X11 XM_011513769.3:c.773-1484…

XM_011513769.3:c.773-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X14 XM_011513771.2:c.377-1484…

XM_011513771.2:c.377-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X3 XM_047449546.1:c.722-1484…

XM_047449546.1:c.722-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X4 XM_047449547.1:c.653-1484…

XM_047449547.1:c.653-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X6 XM_047449548.1:c.653-1484…

XM_047449548.1:c.653-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X7 XM_047449549.1:c.653-1484…

XM_047449549.1:c.653-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X8 XM_047449550.1:c.653-1484…

XM_047449550.1:c.653-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X10 XM_047449551.1:c.758-1484…

XM_047449551.1:c.758-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X12 XM_047449552.1:c.758-1484…

XM_047449552.1:c.758-1484C>T

N/A Intron Variant
PPARGC1A transcript variant X13 XM_047449553.1:c.377-1484…

XM_047449553.1:c.377-1484C>T

N/A Intron Variant
Help

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
Help

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 4 NC_000004.12:g.23825992= NC_000004.12:g.23825992G>A NC_000004.12:g.23825992G>C
GRCh37.p13 chr 4 NC_000004.11:g.23827615= NC_000004.11:g.23827615G>A NC_000004.11:g.23827615G>C
PPARGC1A RefSeqGene NG_028250.2:g.651984= NG_028250.2:g.651984C>T NG_028250.2:g.651984C>G
PPARGC1A transcript variant 1 NM_001330751.2:c.773-1484= NM_001330751.2:c.773-1484C>T NM_001330751.2:c.773-1484C>G
PPARGC1A transcript variant 3 NM_001330752.2:c.722-1484= NM_001330752.2:c.722-1484C>T NM_001330752.2:c.722-1484C>G
PPARGC1A transcript variant 4 NM_001330753.2:c.377-1484= NM_001330753.2:c.377-1484C>T NM_001330753.2:c.377-1484C>G
PPARGC1A transcript variant 5 NM_001354825.2:c.773-1484= NM_001354825.2:c.773-1484C>T NM_001354825.2:c.773-1484C>G
PPARGC1A transcript variant 6 NM_001354826.2:c.377-1484= NM_001354826.2:c.377-1484C>T NM_001354826.2:c.377-1484C>G
PPARGC1A transcript variant 7 NM_001354827.2:c.773-1484= NM_001354827.2:c.773-1484C>T NM_001354827.2:c.773-1484C>G
PPARGC1A transcript NM_013261.3:c.758-1484= NM_013261.3:c.758-1484C>T NM_013261.3:c.758-1484C>G
PPARGC1A transcript variant 2 NM_013261.5:c.758-1484= NM_013261.5:c.758-1484C>T NM_013261.5:c.758-1484C>G
PPARGC1A transcript variant X1 XM_005248130.1:c.773-1484= XM_005248130.1:c.773-1484C>T XM_005248130.1:c.773-1484C>G
PPARGC1A transcript variant X2 XM_005248131.1:c.770-1484= XM_005248131.1:c.770-1484C>T XM_005248131.1:c.770-1484C>G
PPARGC1A transcript variant X1 XM_005248131.6:c.770-1484= XM_005248131.6:c.770-1484C>T XM_005248131.6:c.770-1484C>G
PPARGC1A transcript variant X2 XM_005248132.1:c.749-1484= XM_005248132.1:c.749-1484C>T XM_005248132.1:c.749-1484C>G
PPARGC1A transcript variant X4 XM_005248133.1:c.722-1484= XM_005248133.1:c.722-1484C>T XM_005248133.1:c.722-1484C>G
PPARGC1A transcript variant X5 XM_005248134.1:c.773-1484= XM_005248134.1:c.773-1484C>T XM_005248134.1:c.773-1484C>G
PPARGC1A transcript variant X9 XM_005248134.5:c.773-1484= XM_005248134.5:c.773-1484C>T XM_005248134.5:c.773-1484C>G
PPARGC1A transcript variant X5 XM_011513768.2:c.653-1484= XM_011513768.2:c.653-1484C>T XM_011513768.2:c.653-1484C>G
PPARGC1A transcript variant X11 XM_011513769.3:c.773-1484= XM_011513769.3:c.773-1484C>T XM_011513769.3:c.773-1484C>G
PPARGC1A transcript variant X14 XM_011513771.2:c.377-1484= XM_011513771.2:c.377-1484C>T XM_011513771.2:c.377-1484C>G
PPARGC1A transcript variant X3 XM_047449546.1:c.722-1484= XM_047449546.1:c.722-1484C>T XM_047449546.1:c.722-1484C>G
PPARGC1A transcript variant X4 XM_047449547.1:c.653-1484= XM_047449547.1:c.653-1484C>T XM_047449547.1:c.653-1484C>G
PPARGC1A transcript variant X6 XM_047449548.1:c.653-1484= XM_047449548.1:c.653-1484C>T XM_047449548.1:c.653-1484C>G
PPARGC1A transcript variant X7 XM_047449549.1:c.653-1484= XM_047449549.1:c.653-1484C>T XM_047449549.1:c.653-1484C>G
PPARGC1A transcript variant X8 XM_047449550.1:c.653-1484= XM_047449550.1:c.653-1484C>T XM_047449550.1:c.653-1484C>G
PPARGC1A transcript variant X10 XM_047449551.1:c.758-1484= XM_047449551.1:c.758-1484C>T XM_047449551.1:c.758-1484C>G
PPARGC1A transcript variant X12 XM_047449552.1:c.758-1484= XM_047449552.1:c.758-1484C>T XM_047449552.1:c.758-1484C>G
PPARGC1A transcript variant X13 XM_047449553.1:c.377-1484= XM_047449553.1:c.377-1484C>T XM_047449553.1:c.377-1484C>G
Help

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#.

78 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss4183931 Nov 05, 2001 (101)
2 WI_SSAHASNP ss11659103 Jul 11, 2003 (116)
3 PERLEGEN ss23944557 Sep 20, 2004 (123)
4 ABI ss44497916 Mar 15, 2006 (126)
5 PGA-UW-FHCRC ss79313410 Dec 15, 2007 (130)
6 HUMANGENOME_JCVI ss98942145 Feb 05, 2009 (130)
7 BGI ss105812455 Feb 05, 2009 (130)
8 1000GENOMES ss111935332 Jan 25, 2009 (130)
9 1000GENOMES ss112984774 Jan 25, 2009 (130)
10 ILLUMINA-UK ss116910831 Feb 14, 2009 (130)
11 ENSEMBL ss134766973 Dec 01, 2009 (131)
12 GMI ss156977953 Dec 01, 2009 (131)
13 ILLUMINA ss160603342 Dec 01, 2009 (131)
14 COMPLETE_GENOMICS ss161950243 Jul 04, 2010 (132)
15 COMPLETE_GENOMICS ss163215662 Jul 04, 2010 (132)
16 COMPLETE_GENOMICS ss166296550 Jul 04, 2010 (132)
17 BUSHMAN ss198196352 Jul 04, 2010 (132)
18 BCM-HGSC-SUB ss206267866 Jul 04, 2010 (132)
19 1000GENOMES ss220799150 Jul 14, 2010 (132)
20 1000GENOMES ss232300276 Jul 14, 2010 (132)
21 1000GENOMES ss239613130 Jul 15, 2010 (132)
22 GMI ss277614794 May 04, 2012 (137)
23 GMI ss284864623 Apr 25, 2013 (138)
24 PJP ss293305693 May 09, 2011 (134)
25 ILLUMINA ss481627789 Sep 08, 2015 (146)
26 TISHKOFF ss557376171 Apr 25, 2013 (138)
27 SSMP ss651145481 Apr 25, 2013 (138)
28 EVA-GONL ss979873976 Aug 21, 2014 (142)
29 JMKIDD_LAB ss1071355814 Aug 21, 2014 (142)
30 1000GENOMES ss1308832833 Aug 21, 2014 (142)
31 DDI ss1429806824 Apr 01, 2015 (144)
32 EVA_GENOME_DK ss1580457928 Apr 01, 2015 (144)
33 EVA_DECODE ss1589365202 Apr 01, 2015 (144)
34 EVA_UK10K_ALSPAC ss1609624072 Apr 01, 2015 (144)
35 EVA_UK10K_TWINSUK ss1652618105 Apr 01, 2015 (144)
36 HAMMER_LAB ss1801130599 Sep 08, 2015 (146)
37 WEILL_CORNELL_DGM ss1923109123 Feb 12, 2016 (147)
38 GENOMED ss1969683908 Jul 19, 2016 (147)
39 JJLAB ss2022131756 Sep 14, 2016 (149)
40 CSHL ss2136717994 Nov 08, 2017 (151)
41 USC_VALOUEV ss2150240987 Dec 20, 2016 (150)
42 HUMAN_LONGEVITY ss2261222201 Dec 20, 2016 (150)
43 SYSTEMSBIOZJU ss2625566604 Nov 08, 2017 (151)
44 GRF ss2705689554 Nov 08, 2017 (151)
45 GNOMAD ss2806748361 Nov 08, 2017 (151)
46 SWEGEN ss2994302154 Nov 08, 2017 (151)
47 BIOINF_KMB_FNS_UNIBA ss3024834832 Nov 08, 2017 (151)
48 CSHL ss3345593505 Nov 08, 2017 (151)
49 ILLUMINA ss3636646562 Oct 12, 2018 (152)
50 URBANLAB ss3647674860 Oct 12, 2018 (152)
51 EGCUT_WGS ss3662214862 Jul 13, 2019 (153)
52 EVA_DECODE ss3711607132 Jul 13, 2019 (153)
53 ACPOP ss3730946142 Jul 13, 2019 (153)
54 EVA ss3761525100 Jul 13, 2019 (153)
55 PACBIO ss3784647154 Jul 13, 2019 (153)
56 PACBIO ss3790114196 Jul 13, 2019 (153)
57 PACBIO ss3794989271 Jul 13, 2019 (153)
58 KHV_HUMAN_GENOMES ss3804655892 Jul 13, 2019 (153)
59 EVA ss3828422087 Apr 26, 2020 (154)
60 EVA ss3837644963 Apr 26, 2020 (154)
61 EVA ss3843079461 Apr 26, 2020 (154)
62 SGDP_PRJ ss3858434753 Apr 26, 2020 (154)
63 KRGDB ss3904594069 Apr 26, 2020 (154)
64 KOGIC ss3953715057 Apr 26, 2020 (154)
65 EVA ss3984525064 Apr 26, 2021 (155)
66 TOPMED ss4606235026 Apr 26, 2021 (155)
67 TOMMO_GENOMICS ss5164646145 Apr 26, 2021 (155)
68 1000G_HIGH_COVERAGE ss5258396286 Oct 13, 2022 (156)
69 HUGCELL_USP ss5457259301 Oct 13, 2022 (156)
70 EVA ss5507425280 Oct 13, 2022 (156)
71 1000G_HIGH_COVERAGE ss5539015822 Oct 13, 2022 (156)
72 SANFORD_IMAGENETICS ss5634553658 Oct 13, 2022 (156)
73 TOMMO_GENOMICS ss5698416814 Oct 13, 2022 (156)
74 YY_MCH ss5804848755 Oct 13, 2022 (156)
75 EVA ss5843689201 Oct 13, 2022 (156)
76 EVA ss5854123373 Oct 13, 2022 (156)
77 EVA ss5862548244 Oct 13, 2022 (156)
78 EVA ss5962937770 Oct 13, 2022 (156)
79 1000Genomes NC_000004.11 - 23827615 Oct 12, 2018 (152)
80 1000Genomes_30x NC_000004.12 - 23825992 Oct 13, 2022 (156)
81 The Avon Longitudinal Study of Parents and Children NC_000004.11 - 23827615 Oct 12, 2018 (152)
82 Genetic variation in the Estonian population NC_000004.11 - 23827615 Oct 12, 2018 (152)
83 The Danish reference pan genome NC_000004.11 - 23827615 Apr 26, 2020 (154)
84 gnomAD - Genomes NC_000004.12 - 23825992 Apr 26, 2021 (155)
85 Genome of the Netherlands Release 5 NC_000004.11 - 23827615 Apr 26, 2020 (154)
86 HapMap NC_000004.12 - 23825992 Apr 26, 2020 (154)
87 KOREAN population from KRGDB NC_000004.11 - 23827615 Apr 26, 2020 (154)
88 Korean Genome Project NC_000004.12 - 23825992 Apr 26, 2020 (154)
89 Northern Sweden NC_000004.11 - 23827615 Jul 13, 2019 (153)
90 CNV burdens in cranial meningiomas NC_000004.11 - 23827615 Apr 26, 2021 (155)
91 Qatari NC_000004.11 - 23827615 Apr 26, 2020 (154)
92 SGDP_PRJ NC_000004.11 - 23827615 Apr 26, 2020 (154)
93 Siberian NC_000004.11 - 23827615 Apr 26, 2020 (154)
94 8.3KJPN NC_000004.11 - 23827615 Apr 26, 2021 (155)
95 14KJPN NC_000004.12 - 23825992 Oct 13, 2022 (156)
96 TopMed NC_000004.12 - 23825992 Apr 26, 2021 (155)
97 UK 10K study - Twins NC_000004.11 - 23827615 Oct 12, 2018 (152)
98 A Vietnamese Genetic Variation Database NC_000004.11 - 23827615 Jul 13, 2019 (153)
99 ALFA NC_000004.12 - 23825992 Apr 26, 2021 (155)
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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)
rs58998707 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss111935332, ss112984774, ss116910831, ss161950243, ss163215662, ss166296550, ss198196352, ss206267866, ss277614794, ss284864623, ss293305693, ss1589365202, ss2136717994 NC_000004.10:23436712:G:A NC_000004.12:23825991:G:A (self)
20194778, 11251410, 7953110, 6622867, 4952445, 11771463, 4231007, 74423, 5151053, 10451733, 2757341, 22615452, 11251410, 2462463, ss220799150, ss232300276, ss239613130, ss481627789, ss557376171, ss651145481, ss979873976, ss1071355814, ss1308832833, ss1429806824, ss1580457928, ss1609624072, ss1652618105, ss1801130599, ss1923109123, ss1969683908, ss2022131756, ss2150240987, ss2625566604, ss2705689554, ss2806748361, ss2994302154, ss3345593505, ss3636646562, ss3662214862, ss3730946142, ss3761525100, ss3784647154, ss3790114196, ss3794989271, ss3828422087, ss3837644963, ss3858434753, ss3904594069, ss3984525064, ss5164646145, ss5507425280, ss5634553658, ss5843689201, ss5962937770 NC_000004.11:23827614:G:A NC_000004.12:23825991:G:A (self)
26541757, 143087633, 2575554, 10093058, 32253918, 443612582, 14091541202, ss2261222201, ss3024834832, ss3647674860, ss3711607132, ss3804655892, ss3843079461, ss3953715057, ss4606235026, ss5258396286, ss5457259301, ss5539015822, ss5698416814, ss5804848755, ss5854123373, ss5862548244 NC_000004.12:23825991:G:A NC_000004.12:23825991:G:A (self)
ss11659103 NT_006316.15:14502972:G:A NC_000004.12:23825991:G:A (self)
ss4183931, ss23944557, ss44497916, ss79313410, ss98942145, ss105812455, ss134766973, ss156977953, ss160603342 NT_006316.16:15009411:G:A NC_000004.12:23825991:G:A (self)
11771463, ss3904594069 NC_000004.11:23827614:G:C NC_000004.12:23825991:G:C (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

2 citations for rs2970856
PMID Title Author Year Journal
19828207 Evaluation of the association between the PPARGC1A genetic polymorphisms and type 2 diabetes in Han Chinese population. Zhu S et al. 2009 Diabetes research and clinical practice
29030253 Polymorphisms in the TFAM and PGC1-α genes and their association with polycystic ovary syndrome among South Indian women. Reddy TV et al. 2018 Gene
Help

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.

Software version is: 2.0.1.post761+d5e8e07