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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs7192898

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr16:19069336 (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
T>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.454774 (120374/264690, TOPMED)
T=0.16328 (4614/28258, 14KJPN)
T=0.16342 (2739/16760, 8.3KJPN) (+ 16 more)
G=0.45610 (5818/12756, ALFA)
T=0.4349 (2785/6404, 1000G_30x)
T=0.4247 (2127/5008, 1000G)
T=0.4297 (1925/4480, Estonian)
T=0.3729 (1437/3854, ALSPAC)
T=0.3595 (1333/3708, TWINSUK)
T=0.1679 (492/2930, KOREAN)
T=0.4540 (858/1890, HapMap)
T=0.1730 (317/1832, Korea1K)
T=0.358 (357/998, GoNL)
T=0.357 (214/600, NorthernSweden)
T=0.228 (106/464, SGDP_PRJ)
T=0.329 (71/216, Qatari)
T=0.264 (57/216, Vietnamese)
T=0.18 (9/50, Siberian)
T=0.30 (12/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
COQ7 : Intron Variant
COQ7-DT : 2KB Upstream Variant
Publications
1 citation
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 12756 T=0.54390 C=0.00000, G=0.45610
European Sub 9342 T=0.4700 C=0.0000, G=0.5300
African Sub 2554 T=0.8309 C=0.0000, G=0.1691
African Others Sub 92 T=0.88 C=0.00, G=0.12
African American Sub 2462 T=0.8290 C=0.0000, G=0.1710
Asian Sub 20 T=0.30 C=0.00, G=0.70
East Asian Sub 16 T=0.31 C=0.00, G=0.69
Other Asian Sub 4 T=0.2 C=0.0, G=0.8
Latin American 1 Sub 50 T=0.66 C=0.00, G=0.34
Latin American 2 Sub 116 T=0.672 C=0.000, G=0.328
South Asian Sub 24 T=0.83 C=0.00, G=0.17
Other Sub 650 T=0.443 C=0.000, G=0.557


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 T=0.454774 G=0.545226
14KJPN JAPANESE Study-wide 28258 T=0.16328 G=0.83672
8.3KJPN JAPANESE Study-wide 16760 T=0.16342 G=0.83658
Allele Frequency Aggregator Total Global 12756 T=0.54390 C=0.00000, G=0.45610
Allele Frequency Aggregator European Sub 9342 T=0.4700 C=0.0000, G=0.5300
Allele Frequency Aggregator African Sub 2554 T=0.8309 C=0.0000, G=0.1691
Allele Frequency Aggregator Other Sub 650 T=0.443 C=0.000, G=0.557
Allele Frequency Aggregator Latin American 2 Sub 116 T=0.672 C=0.000, G=0.328
Allele Frequency Aggregator Latin American 1 Sub 50 T=0.66 C=0.00, G=0.34
Allele Frequency Aggregator South Asian Sub 24 T=0.83 C=0.00, G=0.17
Allele Frequency Aggregator Asian Sub 20 T=0.30 C=0.00, G=0.70
1000Genomes_30x Global Study-wide 6404 T=0.4349 G=0.5651
1000Genomes_30x African Sub 1786 T=0.7413 G=0.2587
1000Genomes_30x Europe Sub 1266 T=0.3515 G=0.6485
1000Genomes_30x South Asian Sub 1202 T=0.3561 G=0.6439
1000Genomes_30x East Asian Sub 1170 T=0.1812 G=0.8188
1000Genomes_30x American Sub 980 T=0.384 G=0.616
1000Genomes Global Study-wide 5008 T=0.4247 G=0.5753
1000Genomes African Sub 1322 T=0.7337 G=0.2663
1000Genomes East Asian Sub 1008 T=0.1855 G=0.8145
1000Genomes Europe Sub 1006 T=0.3539 G=0.6461
1000Genomes South Asian Sub 978 T=0.358 G=0.642
1000Genomes American Sub 694 T=0.380 G=0.620
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.4297 G=0.5703
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.3729 G=0.6271
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.3595 G=0.6405
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.1679 G=0.8321
HapMap Global Study-wide 1890 T=0.4540 G=0.5460
HapMap American Sub 770 T=0.405 G=0.595
HapMap African Sub 690 T=0.651 G=0.349
HapMap Asian Sub 254 T=0.161 G=0.839
HapMap Europe Sub 176 T=0.318 G=0.682
Korean Genome Project KOREAN Study-wide 1832 T=0.1730 G=0.8270
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.358 G=0.642
Northern Sweden ACPOP Study-wide 600 T=0.357 G=0.643
SGDP_PRJ Global Study-wide 464 T=0.228 G=0.772
Qatari Global Study-wide 216 T=0.329 G=0.671
A Vietnamese Genetic Variation Database Global Study-wide 216 T=0.264 G=0.736
Siberian Global Study-wide 50 T=0.18 G=0.82
The Danish reference pan genome Danish Study-wide 40 T=0.30 G=0.70
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 16 NC_000016.10:g.19069336T>C
GRCh38.p14 chr 16 NC_000016.10:g.19069336T>G
GRCh37.p13 chr 16 NC_000016.9:g.19080658T>C
GRCh37.p13 chr 16 NC_000016.9:g.19080658T>G
COQ7 RefSeqGene NG_046596.1:g.6742T>C
COQ7 RefSeqGene NG_046596.1:g.6742T>G
Gene: COQ7, coenzyme Q7, hydroxylase (plus strand)
Molecule type Change Amino acid[Codon] SO Term
COQ7 transcript variant 2 NM_001190983.2:c.-42+1328…

NM_001190983.2:c.-42+1328T>C

 		N/A Intron Variant
COQ7 transcript variant 3 NM_001370489.1:c.31+458T>C N/A Intron Variant
COQ7 transcript variant 4 NM_001370490.1:c.73+1599T…

NM_001370490.1:c.73+1599T>C

 		N/A Intron Variant
COQ7 transcript variant 5 NM_001370491.1:c.31+458T>C N/A Intron Variant
COQ7 transcript variant 6 NM_001370492.1:c.-42+1106…

NM_001370492.1:c.-42+1106T>C

 		N/A Intron Variant
COQ7 transcript variant 7 NM_001370493.1:c.-42+1140…

NM_001370493.1:c.-42+1140T>C

 		N/A Intron Variant
COQ7 transcript variant 8 NM_001370494.1:c.-42+1506…

NM_001370494.1:c.-42+1506T>C

 		N/A Intron Variant
COQ7 transcript variant 9 NM_001370495.1:c.-42+1328…

NM_001370495.1:c.-42+1328T>C

 		N/A Intron Variant
COQ7 transcript variant 1 NM_016138.5:c.73+1599T>C N/A Intron Variant
COQ7 transcript variant 10 NR_163448.1:n. N/A Intron Variant
COQ7 transcript variant 11 NR_163449.1:n. N/A Intron Variant
COQ7 transcript variant 12 NR_163450.1:n. N/A Intron Variant
COQ7 transcript variant X1 XM_047433494.1:c.73+1599T…

XM_047433494.1:c.73+1599T>C

 		N/A Intron Variant
COQ7 transcript variant X2 XM_047433495.1:c.73+1599T…

XM_047433495.1:c.73+1599T>C

 		N/A Intron Variant
COQ7 transcript variant X3 XM_047433496.1:c.73+1599T…

XM_047433496.1:c.73+1599T>C

 		N/A Intron Variant
COQ7 transcript variant X4 XM_047433497.1:c.31+458T>C N/A Intron Variant
COQ7 transcript variant X5 XM_047433498.1:c.31+458T>C N/A Intron Variant
Gene: COQ7-DT, COQ7 divergent transcript (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
COQ7-DT transcript variant 1 NR_119379.1:n. N/A Upstream Transcript Variant
COQ7-DT transcript variant 2 NR_119380.1:n. N/A Upstream Transcript Variant
COQ7-DT transcript variant 3 NR_119381.1:n. N/A Upstream Transcript Variant
COQ7-DT transcript variant 4 NR_119382.1:n. N/A Upstream 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

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 T= C G
GRCh38.p14 chr 16 NC_000016.10:g.19069336= NC_000016.10:g.19069336T>C NC_000016.10:g.19069336T>G
GRCh37.p13 chr 16 NC_000016.9:g.19080658= NC_000016.9:g.19080658T>C NC_000016.9:g.19080658T>G
COQ7 RefSeqGene NG_046596.1:g.6742= NG_046596.1:g.6742T>C NG_046596.1:g.6742T>G
COQ7 transcript variant 2 NM_001190983.1:c.-42+1328= NM_001190983.1:c.-42+1328T>C NM_001190983.1:c.-42+1328T>G
COQ7 transcript variant 2 NM_001190983.2:c.-42+1328= NM_001190983.2:c.-42+1328T>C NM_001190983.2:c.-42+1328T>G
COQ7 transcript variant 3 NM_001370489.1:c.31+458= NM_001370489.1:c.31+458T>C NM_001370489.1:c.31+458T>G
COQ7 transcript variant 4 NM_001370490.1:c.73+1599= NM_001370490.1:c.73+1599T>C NM_001370490.1:c.73+1599T>G
COQ7 transcript variant 5 NM_001370491.1:c.31+458= NM_001370491.1:c.31+458T>C NM_001370491.1:c.31+458T>G
COQ7 transcript variant 6 NM_001370492.1:c.-42+1106= NM_001370492.1:c.-42+1106T>C NM_001370492.1:c.-42+1106T>G
COQ7 transcript variant 7 NM_001370493.1:c.-42+1140= NM_001370493.1:c.-42+1140T>C NM_001370493.1:c.-42+1140T>G
COQ7 transcript variant 8 NM_001370494.1:c.-42+1506= NM_001370494.1:c.-42+1506T>C NM_001370494.1:c.-42+1506T>G
COQ7 transcript variant 9 NM_001370495.1:c.-42+1328= NM_001370495.1:c.-42+1328T>C NM_001370495.1:c.-42+1328T>G
COQ7 transcript variant 1 NM_016138.4:c.73+1599= NM_016138.4:c.73+1599T>C NM_016138.4:c.73+1599T>G
COQ7 transcript variant 1 NM_016138.5:c.73+1599= NM_016138.5:c.73+1599T>C NM_016138.5:c.73+1599T>G
COQ7 transcript variant X1 XM_005255033.1:c.31+458= XM_005255033.1:c.31+458T>C XM_005255033.1:c.31+458T>G
COQ7 transcript variant X1 XM_047433494.1:c.73+1599= XM_047433494.1:c.73+1599T>C XM_047433494.1:c.73+1599T>G
COQ7 transcript variant X2 XM_047433495.1:c.73+1599= XM_047433495.1:c.73+1599T>C XM_047433495.1:c.73+1599T>G
COQ7 transcript variant X3 XM_047433496.1:c.73+1599= XM_047433496.1:c.73+1599T>C XM_047433496.1:c.73+1599T>G
COQ7 transcript variant X4 XM_047433497.1:c.31+458= XM_047433497.1:c.31+458T>C XM_047433497.1:c.31+458T>G
COQ7 transcript variant X5 XM_047433498.1:c.31+458= XM_047433498.1:c.31+458T>C XM_047433498.1:c.31+458T>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#.

80 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss10820401 Jul 11, 2003 (116)
2 CSHL-HAPMAP ss16699767 Feb 27, 2004 (120)
3 CSHL-HAPMAP ss20016266 Feb 27, 2004 (120)
4 SSAHASNP ss21319895 Apr 05, 2004 (123)
5 ABI ss40711691 Mar 14, 2006 (126)
6 ILLUMINA ss75175701 Dec 06, 2007 (129)
7 BCMHGSC_JDW ss90341410 Mar 24, 2008 (129)
8 HUMANGENOME_JCVI ss96672475 Feb 05, 2009 (130)
9 BGI ss106465071 Feb 05, 2009 (130)
10 1000GENOMES ss109246155 Jan 23, 2009 (130)
11 ENSEMBL ss136621816 Dec 01, 2009 (131)
12 ENSEMBL ss136780284 Dec 01, 2009 (131)
13 GMI ss157170655 Dec 01, 2009 (131)
14 COMPLETE_GENOMICS ss167976817 Jul 04, 2010 (132)
15 ILLUMINA ss174283096 Jul 04, 2010 (132)
16 BUSHMAN ss201521647 Jul 04, 2010 (132)
17 1000GENOMES ss227178316 Jul 14, 2010 (132)
18 1000GENOMES ss236978495 Jul 15, 2010 (132)
19 1000GENOMES ss243327742 Jul 15, 2010 (132)
20 BL ss255565550 May 09, 2011 (134)
21 GMI ss282464585 May 04, 2012 (137)
22 GMI ss287046424 Apr 25, 2013 (138)
23 PJP ss291931582 May 09, 2011 (134)
24 ILLUMINA ss537448128 Sep 08, 2015 (146)
25 TISHKOFF ss564825061 Apr 25, 2013 (138)
26 SSMP ss660573546 Apr 25, 2013 (138)
27 EVA-GONL ss992354261 Aug 21, 2014 (142)
28 JMKIDD_LAB ss1080536265 Aug 21, 2014 (142)
29 1000GENOMES ss1355663450 Aug 21, 2014 (142)
30 DDI ss1427800119 Apr 01, 2015 (144)
31 EVA_GENOME_DK ss1577865107 Apr 01, 2015 (144)
32 EVA_UK10K_ALSPAC ss1634148710 Apr 01, 2015 (144)
33 EVA_UK10K_TWINSUK ss1677142743 Apr 01, 2015 (144)
34 EVA_DECODE ss1696388240 Apr 01, 2015 (144)
35 EVA_SVP ss1713530679 Apr 01, 2015 (144)
36 HAMMER_LAB ss1808453773 Sep 08, 2015 (146)
37 WEILL_CORNELL_DGM ss1935775355 Feb 12, 2016 (147)
38 GENOMED ss1968235558 Jul 19, 2016 (147)
39 JJLAB ss2028674736 Sep 14, 2016 (149)
40 USC_VALOUEV ss2157084799 Dec 20, 2016 (150)
41 HUMAN_LONGEVITY ss2211135576 Dec 20, 2016 (150)
42 SYSTEMSBIOZJU ss2628830274 Nov 08, 2017 (151)
43 ILLUMINA ss2635062925 Nov 08, 2017 (151)
44 GRF ss2701587967 Nov 08, 2017 (151)
45 GNOMAD ss2941151726 Nov 08, 2017 (151)
46 SWEGEN ss3014193772 Nov 08, 2017 (151)
47 BIOINF_KMB_FNS_UNIBA ss3028161776 Nov 08, 2017 (151)
48 CSHL ss3351371935 Nov 08, 2017 (151)
49 ILLUMINA ss3627493004 Oct 12, 2018 (152)
50 ILLUMINA ss3638117393 Oct 12, 2018 (152)
51 ILLUMINA ss3643099083 Oct 12, 2018 (152)
52 URBANLAB ss3650481043 Oct 12, 2018 (152)
53 EGCUT_WGS ss3681290145 Jul 13, 2019 (153)
54 EVA_DECODE ss3698977269 Jul 13, 2019 (153)
55 ACPOP ss3741397733 Jul 13, 2019 (153)
56 EVA ss3753769455 Jul 13, 2019 (153)
57 PACBIO ss3788000732 Jul 13, 2019 (153)
58 PACBIO ss3792991322 Jul 13, 2019 (153)
59 PACBIO ss3797876287 Jul 13, 2019 (153)
60 KHV_HUMAN_GENOMES ss3819064493 Jul 13, 2019 (153)
61 EVA ss3834508873 Apr 27, 2020 (154)
62 EVA ss3840861682 Apr 27, 2020 (154)
63 EVA ss3846352543 Apr 27, 2020 (154)
64 SGDP_PRJ ss3884107921 Apr 27, 2020 (154)
65 KRGDB ss3933425144 Apr 27, 2020 (154)
66 KOGIC ss3977230091 Apr 27, 2020 (154)
67 TOPMED ss5010128427 Apr 26, 2021 (155)
68 TOMMO_GENOMICS ss5218779395 Apr 26, 2021 (155)
69 1000G_HIGH_COVERAGE ss5300395439 Oct 16, 2022 (156)
70 HUGCELL_USP ss5493871997 Oct 16, 2022 (156)
71 EVA ss5511582037 Oct 16, 2022 (156)
72 1000G_HIGH_COVERAGE ss5602747197 Oct 16, 2022 (156)
73 SANFORD_IMAGENETICS ss5658612715 Oct 16, 2022 (156)
74 TOMMO_GENOMICS ss5773362630 Oct 16, 2022 (156)
75 YY_MCH ss5815823069 Oct 16, 2022 (156)
76 EVA ss5846202129 Oct 16, 2022 (156)
77 EVA ss5851519243 Oct 16, 2022 (156)
78 EVA ss5898546435 Oct 16, 2022 (156)
79 EVA ss5950032277 Oct 16, 2022 (156)
80 EVA ss5980910376 Oct 16, 2022 (156)
81 1000Genomes NC_000016.9 - 19080658 Oct 12, 2018 (152)
82 1000Genomes_30x NC_000016.10 - 19069336 Oct 16, 2022 (156)
83 The Avon Longitudinal Study of Parents and Children NC_000016.9 - 19080658 Oct 12, 2018 (152)
84 Genetic variation in the Estonian population NC_000016.9 - 19080658 Oct 12, 2018 (152)
85 The Danish reference pan genome NC_000016.9 - 19080658 Apr 27, 2020 (154)
86 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 484905386 (NC_000016.10:19069335:T:C 2/139580)
Row 484905387 (NC_000016.10:19069335:T:G 75996/139490)

- Apr 26, 2021 (155)
87 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 484905386 (NC_000016.10:19069335:T:C 2/139580)
Row 484905387 (NC_000016.10:19069335:T:G 75996/139490)

- Apr 26, 2021 (155)
88 Genome of the Netherlands Release 5 NC_000016.9 - 19080658 Apr 27, 2020 (154)
89 HapMap NC_000016.10 - 19069336 Apr 27, 2020 (154)
90 KOREAN population from KRGDB NC_000016.9 - 19080658 Apr 27, 2020 (154)
91 Korean Genome Project NC_000016.10 - 19069336 Apr 27, 2020 (154)
92 Northern Sweden NC_000016.9 - 19080658 Jul 13, 2019 (153)
93 Qatari NC_000016.9 - 19080658 Apr 27, 2020 (154)
94 SGDP_PRJ NC_000016.9 - 19080658 Apr 27, 2020 (154)
95 Siberian NC_000016.9 - 19080658 Apr 27, 2020 (154)
96 8.3KJPN NC_000016.9 - 19080658 Apr 26, 2021 (155)
97 14KJPN NC_000016.10 - 19069336 Oct 16, 2022 (156)
98 TopMed NC_000016.10 - 19069336 Apr 26, 2021 (155)
99 UK 10K study - Twins NC_000016.9 - 19080658 Oct 12, 2018 (152)
100 A Vietnamese Genetic Variation Database NC_000016.9 - 19080658 Jul 13, 2019 (153)
101 ALFA NC_000016.10 - 19069336 Apr 26, 2021 (155)
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)
rs12922555 Sep 24, 2004 (123)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
5933677309 NC_000016.10:19069335:T:C NC_000016.10:19069335:T:C (self)
ss90341410, ss109246155, ss167976817, ss201521647, ss255565550, ss282464585, ss287046424, ss291931582, ss1696388240, ss1713530679, ss2635062925, ss3643099083 NC_000016.8:18988158:T:G NC_000016.10:19069335:T:G (self)
68807306, 38196925, 27028393, 4079469, 17040111, 40602538, 14682598, 17817277, 36124901, 9601153, 76748702, 38196925, 8484941, ss227178316, ss236978495, ss243327742, ss537448128, ss564825061, ss660573546, ss992354261, ss1080536265, ss1355663450, ss1427800119, ss1577865107, ss1634148710, ss1677142743, ss1808453773, ss1935775355, ss1968235558, ss2028674736, ss2157084799, ss2628830274, ss2701587967, ss2941151726, ss3014193772, ss3351371935, ss3627493004, ss3638117393, ss3681290145, ss3741397733, ss3753769455, ss3788000732, ss3792991322, ss3797876287, ss3834508873, ss3840861682, ss3884107921, ss3933425144, ss5218779395, ss5511582037, ss5658612715, ss5846202129, ss5950032277, ss5980910376 NC_000016.9:19080657:T:G NC_000016.10:19069335:T:G (self)
90273132, 1361615, 33608092, 107199734, 225674088, 5933677309, ss2211135576, ss3028161776, ss3650481043, ss3698977269, ss3819064493, ss3846352543, ss3977230091, ss5010128427, ss5300395439, ss5493871997, ss5602747197, ss5773362630, ss5815823069, ss5851519243, ss5898546435 NC_000016.10:19069335:T:G NC_000016.10:19069335:T:G (self)
ss10820401 NT_010393.13:10353875:T:G NC_000016.10:19069335:T:G (self)
ss16699767, ss20016266, ss21319895 NT_010393.14:10392990:T:G NC_000016.10:19069335:T:G (self)
ss40711691, ss75175701, ss96672475, ss106465071, ss136621816, ss136780284, ss157170655, ss174283096 NT_010393.16:19020657:T:G NC_000016.10:19069335:T:G (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.

1 citation for rs7192898
PMID Title Author Year Journal
18765803 FOXO3A genotype is strongly associated with human longevity. Willcox BJ et al. 2008 Proceedings of the National Academy of Sciences of the United States of America
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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