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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 Aliases 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.

rs9931441

Current Build 153

Released July 9, 2019

Organism
Homo sapiens
Position
chr16:10480956 (GRCh38.p12) 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
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.04764 (11972/251280, GnomAD_exome)
A=0.07578 (9515/125568, TOPMED)
A=0.05229 (6346/121354, ExAC) (+ 9 more)
A=0.1105 (8697/78700, PAGE_STUDY)
A=0.0681 (2137/31378, GnomAD)
A=0.0753 (979/12994, GO-ESP)
A=0.101 (507/5008, 1000G)
A=0.014 (63/4480, Estonian)
A=0.022 (84/3854, ALSPAC)
A=0.024 (90/3708, TWINSUK)
A=0.16 (101/616, Vietnamese)
A=0.02 (13/600, NorthernSweden)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ATF7IP2 : Missense Variant
Publications
0 citations
Genomic View
See rs on genome
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.p12 chr 16 NC_000016.10:g.10480956G>A
GRCh37.p13 chr 16 NC_000016.9:g.10574813G>A
Gene: ATF7IP2, activating transcription factor 7 interacting protein 2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ATF7IP2 transcript variant 5 NM_001352120.2:c.1627G>A A [GCA] > T [ACA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform 1 NP_001339049.1:p.Ala543Thr A (Ala) > T (Thr) Missense Variant
ATF7IP2 transcript variant 2 NM_001256160.3:c.1560G>A M [ATG] > I [ATA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform 2 NP_001243089.1:p.Met520Ile M (Met) > I (Ile) Missense Variant
ATF7IP2 transcript variant 1 NM_024997.5:c.1627G>A A [GCA] > T [ACA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform 1 NP_079273.2:p.Ala543Thr A (Ala) > T (Thr) Missense Variant
ATF7IP2 transcript variant 3 NR_045815.2:n.1752G>A N/A Non Coding Transcript Variant
ATF7IP2 transcript variant 4 NR_045816.2:n.1678G>A N/A Non Coding Transcript Variant
ATF7IP2 transcript variant 6 NR_147927.1:n.1795G>A N/A Non Coding Transcript Variant
ATF7IP2 transcript variant X6 XM_017023707.2:c.*103= N/A 3 Prime UTR Variant
ATF7IP2 transcript variant X9 XM_006720954.4:c. N/A Genic Downstream Transcript Variant
ATF7IP2 transcript variant X2 XM_006720953.3:c.1627G>A A [GCA] > T [ACA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform X1 XP_006721016.1:p.Ala543Thr A (Ala) > T (Thr) Missense Variant
ATF7IP2 transcript variant X8 XM_017023708.1:c.772G>A A [GCA] > T [ACA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform X4 XP_016879197.1:p.Ala258Thr A (Ala) > T (Thr) Missense Variant
ATF7IP2 transcript variant X10 XM_017023709.1:c.463G>A A [GCA] > T [ACA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform X6 XP_016879198.1:p.Ala155Thr A (Ala) > T (Thr) Missense Variant
ATF7IP2 transcript variant X11 XM_011522666.2:c.463G>A A [GCA] > T [ACA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform X6 XP_011520968.1:p.Ala155Thr A (Ala) > T (Thr) Missense Variant
ATF7IP2 transcript variant X12 XM_017023710.1:c.460G>A A [GCA] > T [ACA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform X7 XP_016879199.1:p.Ala154Thr A (Ala) > T (Thr) Missense Variant
ATF7IP2 transcript variant X13 XM_017023711.1:c.289G>A A [GCA] > T [ACA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform X8 XP_016879200.1:p.Ala97Thr A (Ala) > T (Thr) Missense Variant
ATF7IP2 transcript variant X1 XM_017023705.2:c.1627G>A A [GCA] > T [ACA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform X1 XP_016879194.1:p.Ala543Thr A (Ala) > T (Thr) Missense Variant
ATF7IP2 transcript variant X3 XM_017023706.2:c.1560G>A M [ATG] > I [ATA] Coding Sequence Variant
activating transcription factor 7-interacting protein 2 isoform X2 XP_016879195.1:p.Met520Ile M (Met) > I (Ile) Missense Variant
ATF7IP2 transcript variant X4 XR_001751990.1:n.2747G>A N/A Non Coding Transcript Variant
ATF7IP2 transcript variant X5 XR_001751991.1:n.1813G>A N/A Non Coding Transcript Variant
ATF7IP2 transcript variant X7 XR_001751992.2:n.2588G>A N/A Non Coding Transcript 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

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
gnomAD - Exomes Global Study-wide 251280 G=0.95236 A=0.04764
gnomAD - Exomes European Sub 135310 G=0.97999 A=0.02001
gnomAD - Exomes Asian Sub 48948 G=0.9002 A=0.0998
gnomAD - Exomes American Sub 34580 G=0.9800 A=0.0200
gnomAD - Exomes African Sub 16242 G=0.8226 A=0.1774
gnomAD - Exomes Ashkenazi Jewish Sub 10068 G=0.9445 A=0.0555
gnomAD - Exomes Other Sub 6132 G=0.959 A=0.041
TopMed Global Study-wide 125568 G=0.92422 A=0.07578
ExAC Global Study-wide 121354 G=0.94771 A=0.05229
ExAC Europe Sub 73326 G=0.9769 A=0.0231
ExAC Asian Sub 25148 G=0.9015 A=0.0985
ExAC American Sub 11574 G=0.9785 A=0.0215
ExAC African Sub 10398 G=0.8188 A=0.1812
ExAC Other Sub 908 G=0.95 A=0.05
The PAGE Study Global Study-wide 78700 G=0.8895 A=0.1105
The PAGE Study AfricanAmerican Sub 32514 G=0.8377 A=0.1623
The PAGE Study Mexican Sub 10810 G=0.9757 A=0.0243
The PAGE Study Asian Sub 8318 G=0.834 A=0.166
The PAGE Study PuertoRican Sub 7918 G=0.949 A=0.051
The PAGE Study NativeHawaiian Sub 4534 G=0.879 A=0.121
The PAGE Study Cuban Sub 4230 G=0.950 A=0.050
The PAGE Study Dominican Sub 3828 G=0.914 A=0.086
The PAGE Study CentralAmerican Sub 2450 G=0.962 A=0.038
The PAGE Study SouthAmerican Sub 1982 G=0.972 A=0.028
The PAGE Study NativeAmerican Sub 1260 G=0.963 A=0.037
The PAGE Study SouthAsian Sub 856 G=0.90 A=0.10
gnomAD - Genomes Global Study-wide 31378 G=0.9319 A=0.0681
gnomAD - Genomes European Sub 18898 G=0.9820 A=0.0180
gnomAD - Genomes African Sub 8698 G=0.827 A=0.173
gnomAD - Genomes East Asian Sub 1556 G=0.866 A=0.134
gnomAD - Genomes Other Sub 1088 G=0.967 A=0.033
gnomAD - Genomes American Sub 848 G=0.97 A=0.03
gnomAD - Genomes Ashkenazi Jewish Sub 290 G=0.93 A=0.07
GO Exome Sequencing Project Global Study-wide 12994 G=0.9247 A=0.0753
GO Exome Sequencing Project European American Sub 8600 G=0.976 A=0.024
GO Exome Sequencing Project African American Sub 4394 G=0.824 A=0.176
1000Genomes Global Study-wide 5008 G=0.899 A=0.101
1000Genomes African Sub 1322 G=0.808 A=0.192
1000Genomes East Asian Sub 1008 G=0.874 A=0.126
1000Genomes Europe Sub 1006 G=0.978 A=0.022
1000Genomes South Asian Sub 978 G=0.91 A=0.09
1000Genomes American Sub 694 G=0.98 A=0.02
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.986 A=0.014
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.978 A=0.022
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.976 A=0.024
A Vietnamese Genetic Variation Database Global Study-wide 616 G=0.84 A=0.16
Northern Sweden ACPOP Study-wide 600 G=0.98 A=0.02
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 Note
GRCh38.p12 chr 16 NC_000016.10:g.10480956= NC_000016.10:g.10480956G>A
GRCh37.p13 chr 16 NC_000016.9:g.10574813= NC_000016.9:g.10574813G>A
ATF7IP2 transcript variant 1 NM_024997.4:c.1627= NM_024997.4:c.1627G>A
ATF7IP2 transcript variant 1 NM_024997.5:c.1627= NM_024997.5:c.1627G>A
ATF7IP2 transcript variant 1 NM_024997.3:c.1627= NM_024997.3:c.1627G>A
ATF7IP2 transcript variant X2 XM_006720953.3:c.1627= XM_006720953.3:c.1627G>A
ATF7IP2 transcript variant X1 XM_017023705.2:c.1627= XM_017023705.2:c.1627G>A
ATF7IP2 transcript variant X3 XM_017023706.2:c.1560= XM_017023706.2:c.1560G>A
ATF7IP2 transcript variant X7 XR_001751992.2:n.2588= XR_001751992.2:n.2588G>A
ATF7IP2 transcript variant 2 NM_001256160.2:c.1560= NM_001256160.2:c.1560G>A
ATF7IP2 transcript variant 2 NM_001256160.3:c.1560= NM_001256160.3:c.1560G>A
ATF7IP2 transcript variant 2 NM_001256160.1:c.1560= NM_001256160.1:c.1560G>A
ATF7IP2 transcript variant 3 NR_045815.2:n.1752= NR_045815.2:n.1752G>A
ATF7IP2 transcript variant 3 NR_045815.1:n.1628= NR_045815.1:n.1628G>A
ATF7IP2 transcript variant 4 NR_045816.2:n.1678= NR_045816.2:n.1678G>A
ATF7IP2 transcript variant 4 NR_045816.1:n.1622= NR_045816.1:n.1622G>A
ATF7IP2 transcript variant X6 XM_017023707.2:c.*103= XM_017023707.2:c.*103G>A
ATF7IP2 transcript variant X11 XM_011522666.2:c.463= XM_011522666.2:c.463G>A
ATF7IP2 transcript variant X4 XR_001751990.1:n.2747= XR_001751990.1:n.2747G>A
ATF7IP2 transcript variant 5 NM_001352120.1:c.1627= NM_001352120.1:c.1627G>A
ATF7IP2 transcript variant 5 NM_001352120.2:c.1627= NM_001352120.2:c.1627G>A
ATF7IP2 transcript variant X5 XR_001751991.1:n.1813= XR_001751991.1:n.1813G>A
ATF7IP2 transcript variant 6 NR_147927.1:n.1795= NR_147927.1:n.1795G>A
ATF7IP2 transcript variant X12 XM_017023710.1:c.460= XM_017023710.1:c.460G>A
ATF7IP2 transcript variant X10 XM_017023709.1:c.463= XM_017023709.1:c.463G>A
ATF7IP2 transcript variant X8 XM_017023708.1:c.772= XM_017023708.1:c.772G>A
ATF7IP2 transcript variant X13 XM_017023711.1:c.289= XM_017023711.1:c.289G>A
activating transcription factor 7-interacting protein 2 isoform 1 NP_079273.2:p.Ala543= NP_079273.2:p.Ala543Thr
activating transcription factor 7-interacting protein 2 isoform X1 XP_006721016.1:p.Ala543= XP_006721016.1:p.Ala543Thr
activating transcription factor 7-interacting protein 2 isoform X1 XP_016879194.1:p.Ala543= XP_016879194.1:p.Ala543Thr
activating transcription factor 7-interacting protein 2 isoform X2 XP_016879195.1:p.Met520= XP_016879195.1:p.Met520Ile
activating transcription factor 7-interacting protein 2 isoform 2 NP_001243089.1:p.Met520= NP_001243089.1:p.Met520Ile
activating transcription factor 7-interacting protein 2 isoform X6 XP_011520968.1:p.Ala155= XP_011520968.1:p.Ala155Thr
activating transcription factor 7-interacting protein 2 isoform 1 NP_001339049.1:p.Ala543= NP_001339049.1:p.Ala543Thr
activating transcription factor 7-interacting protein 2 isoform X7 XP_016879199.1:p.Ala154= XP_016879199.1:p.Ala154Thr
activating transcription factor 7-interacting protein 2 isoform X6 XP_016879198.1:p.Ala155= XP_016879198.1:p.Ala155Thr
activating transcription factor 7-interacting protein 2 isoform X4 XP_016879197.1:p.Ala258= XP_016879197.1:p.Ala258Thr
activating transcription factor 7-interacting protein 2 isoform X8 XP_016879200.1:p.Ala97= XP_016879200.1:p.Ala97Thr
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#.

99 SubSNP, 12 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss13770426 Dec 05, 2003 (119)
2 SC_SNP ss15995646 Feb 27, 2004 (120)
3 PERLEGEN ss23754813 Sep 20, 2004 (123)
4 APPLERA_GI ss48407474 Mar 13, 2006 (126)
5 ILLUMINA ss65730235 Oct 16, 2006 (127)
6 PERLEGEN ss69339041 May 18, 2007 (127)
7 AFFY ss74813203 Aug 16, 2007 (128)
8 ILLUMINA ss74861592 Dec 07, 2007 (129)
9 ILLUMINA-UK ss118193207 Feb 14, 2009 (130)
10 SEATTLESEQ ss159732247 Dec 01, 2009 (131)
11 ILLUMINA ss161025808 Dec 01, 2009 (131)
12 ILLUMINA ss174930605 Jul 04, 2010 (132)
13 BUSHMAN ss201446226 Jul 04, 2010 (132)
14 1000GENOMES ss211684755 Jul 14, 2010 (132)
15 1000GENOMES ss227146249 Jul 14, 2010 (132)
16 1000GENOMES ss243309138 Jul 15, 2010 (132)
17 GMI ss282439085 May 04, 2012 (137)
18 PJP ss291919854 May 09, 2011 (134)
19 NHLBI-ESP ss342420778 May 09, 2011 (134)
20 ILLUMINA ss482021006 May 04, 2012 (137)
21 ILLUMINA ss482055225 May 04, 2012 (137)
22 ILLUMINA ss483005449 Sep 08, 2015 (146)
23 ILLUMINA ss485804001 May 04, 2012 (137)
24 1000GENOMES ss491097276 May 04, 2012 (137)
25 EXOME_CHIP ss491504374 May 04, 2012 (137)
26 CLINSEQ_SNP ss491713092 May 04, 2012 (137)
27 ILLUMINA ss537644707 Sep 08, 2015 (146)
28 TISHKOFF ss564785333 Apr 25, 2013 (138)
29 SSMP ss660530049 Apr 25, 2013 (138)
30 ILLUMINA ss778651927 Sep 08, 2015 (146)
31 ILLUMINA ss780715848 Sep 08, 2015 (146)
32 ILLUMINA ss783347851 Sep 08, 2015 (146)
33 ILLUMINA ss783391182 Sep 08, 2015 (146)
34 ILLUMINA ss784299112 Sep 08, 2015 (146)
35 ILLUMINA ss832609823 Sep 08, 2015 (146)
36 ILLUMINA ss834109768 Sep 08, 2015 (146)
37 JMKIDD_LAB ss974494001 Aug 21, 2014 (142)
38 EVA-GONL ss992288035 Aug 21, 2014 (142)
39 JMKIDD_LAB ss1067559110 Aug 21, 2014 (142)
40 JMKIDD_LAB ss1080490915 Aug 21, 2014 (142)
41 1000GENOMES ss1355404233 Aug 21, 2014 (142)
42 EVA_FINRISK ss1584098304 Apr 01, 2015 (144)
43 EVA_UK10K_ALSPAC ss1634021237 Apr 01, 2015 (144)
44 EVA_UK10K_TWINSUK ss1677015270 Apr 01, 2015 (144)
45 EVA_EXAC ss1692151807 Apr 01, 2015 (144)
46 EVA_DECODE ss1696323829 Apr 01, 2015 (144)
47 EVA_MGP ss1711418735 Apr 01, 2015 (144)
48 EVA_SVP ss1713526340 Apr 01, 2015 (144)
49 ILLUMINA ss1752181250 Sep 08, 2015 (146)
50 ILLUMINA ss1752181251 Sep 08, 2015 (146)
51 HAMMER_LAB ss1808425239 Sep 08, 2015 (146)
52 ILLUMINA ss1917904497 Feb 12, 2016 (147)
53 WEILL_CORNELL_DGM ss1935703415 Feb 12, 2016 (147)
54 ILLUMINA ss1946409096 Feb 12, 2016 (147)
55 ILLUMINA ss1959659599 Feb 12, 2016 (147)
56 USC_VALOUEV ss2157049633 Dec 20, 2016 (150)
57 HUMAN_LONGEVITY ss2210664188 Dec 20, 2016 (150)
58 TOPMED ss2375308849 Dec 20, 2016 (150)
59 SYSTEMSBIOZJU ss2628813480 Nov 08, 2017 (151)
60 ILLUMINA ss2633295483 Nov 08, 2017 (151)
61 GRF ss2701545164 Nov 08, 2017 (151)
62 GNOMAD ss2741745074 Nov 08, 2017 (151)
63 GNOMAD ss2749465234 Nov 08, 2017 (151)
64 GNOMAD ss2940362543 Nov 08, 2017 (151)
65 SWEGEN ss3014073656 Nov 08, 2017 (151)
66 ILLUMINA ss3021684617 Nov 08, 2017 (151)
67 TOPMED ss3240180299 Nov 08, 2017 (151)
68 CSHL ss3351340231 Nov 08, 2017 (151)
69 ILLUMINA ss3627479681 Oct 12, 2018 (152)
70 ILLUMINA ss3631283653 Oct 12, 2018 (152)
71 ILLUMINA ss3633114403 Oct 12, 2018 (152)
72 ILLUMINA ss3633820087 Oct 12, 2018 (152)
73 ILLUMINA ss3634632564 Oct 12, 2018 (152)
74 ILLUMINA ss3634632565 Oct 12, 2018 (152)
75 ILLUMINA ss3635508560 Oct 12, 2018 (152)
76 ILLUMINA ss3636322327 Oct 12, 2018 (152)
77 ILLUMINA ss3637259957 Oct 12, 2018 (152)
78 ILLUMINA ss3638113870 Oct 12, 2018 (152)
79 ILLUMINA ss3640339884 Oct 12, 2018 (152)
80 ILLUMINA ss3640339885 Oct 12, 2018 (152)
81 ILLUMINA ss3643095812 Oct 12, 2018 (152)
82 ILLUMINA ss3644662172 Oct 12, 2018 (152)
83 OMUKHERJEE_ADBS ss3646486165 Oct 12, 2018 (152)
84 ILLUMINA ss3652089272 Oct 12, 2018 (152)
85 EGCUT_WGS ss3681196763 Jul 13, 2019 (153)
86 EVA_DECODE ss3698849573 Jul 13, 2019 (153)
87 ILLUMINA ss3725544496 Jul 13, 2019 (153)
88 ACPOP ss3741340879 Jul 13, 2019 (153)
89 ILLUMINA ss3744428693 Jul 13, 2019 (153)
90 ILLUMINA ss3744933024 Jul 13, 2019 (153)
91 ILLUMINA ss3744933025 Jul 13, 2019 (153)
92 EVA ss3753693022 Jul 13, 2019 (153)
93 PAGE_CC ss3771866310 Jul 13, 2019 (153)
94 ILLUMINA ss3772431395 Jul 13, 2019 (153)
95 ILLUMINA ss3772431396 Jul 13, 2019 (153)
96 PACBIO ss3787982169 Jul 13, 2019 (153)
97 PACBIO ss3792975094 Jul 13, 2019 (153)
98 PACBIO ss3797860054 Jul 13, 2019 (153)
99 KHV_HUMAN_GENOMES ss3818989499 Jul 13, 2019 (153)
100 1000Genomes NC_000016.9 - 10574813 Oct 12, 2018 (152)
101 The Avon Longitudinal Study of Parents and Children NC_000016.9 - 10574813 Oct 12, 2018 (152)
102 Genetic variation in the Estonian population NC_000016.9 - 10574813 Oct 12, 2018 (152)
103 ExAC NC_000016.9 - 10574813 Oct 12, 2018 (152)
104 gnomAD - Genomes NC_000016.9 - 10574813 Jul 13, 2019 (153)
105 gnomAD - Exomes NC_000016.9 - 10574813 Jul 13, 2019 (153)
106 GO Exome Sequencing Project NC_000016.9 - 10574813 Oct 12, 2018 (152)
107 Northern Sweden NC_000016.9 - 10574813 Jul 13, 2019 (153)
108 The PAGE Study NC_000016.10 - 10480956 Jul 13, 2019 (153)
109 TopMed NC_000016.10 - 10480956 Oct 12, 2018 (152)
110 UK 10K study - Twins NC_000016.9 - 10574813 Oct 12, 2018 (152)
111 A Vietnamese Genetic Variation Database NC_000016.9 - 10574813 Jul 13, 2019 (153)
Help

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)
rs52793507 Sep 21, 2007 (128)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss118193207, ss201446226, ss211684755, ss282439085, ss291919854, ss482021006, ss491713092, ss1696323829, ss1713526340, ss3643095812 NC_000016.8:10482313:G:A NC_000016.10:10480955:G:A (self)
68539820, 38056422, 26935011, 2548251, 187005710, 11022634, 1444340, 14625744, 38056422, 8457052, ss227146249, ss243309138, ss342420778, ss482055225, ss483005449, ss485804001, ss491097276, ss491504374, ss537644707, ss564785333, ss660530049, ss778651927, ss780715848, ss783347851, ss783391182, ss784299112, ss832609823, ss834109768, ss974494001, ss992288035, ss1067559110, ss1080490915, ss1355404233, ss1584098304, ss1634021237, ss1677015270, ss1692151807, ss1711418735, ss1752181250, ss1752181251, ss1808425239, ss1917904497, ss1935703415, ss1946409096, ss1959659599, ss2157049633, ss2375308849, ss2628813480, ss2633295483, ss2701545164, ss2741745074, ss2749465234, ss2940362543, ss3014073656, ss3021684617, ss3351340231, ss3627479681, ss3631283653, ss3633114403, ss3633820087, ss3634632564, ss3634632565, ss3635508560, ss3636322327, ss3637259957, ss3638113870, ss3640339884, ss3640339885, ss3644662172, ss3646486165, ss3652089272, ss3681196763, ss3741340879, ss3744428693, ss3744933024, ss3744933025, ss3753693022, ss3772431395, ss3772431396, ss3787982169, ss3792975094, ss3797860054 NC_000016.9:10574812:G:A NC_000016.10:10480955:G:A (self)
1087779, 139703226, ss2210664188, ss3240180299, ss3698849573, ss3725544496, ss3771866310, ss3818989499 NC_000016.10:10480955:G:A NC_000016.10:10480955:G:A (self)
ss13770426, ss15995646 NT_010393.14:1887137:G:A NC_000016.10:10480955:G:A (self)
ss23754813, ss48407474, ss65730235, ss69339041, ss74813203, ss74861592, ss159732247, ss161025808, ss174930605 NT_010393.16:10514812:G:A NC_000016.10:10480955:G:A (self)
Help

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

No publications for rs9931441

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.post308+0fe9b3b