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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.

rs515910

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr10:104206646 (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
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.477918 (126500/264690, TOPMED)
G=0.414476 (79368/191490, ALFA)
G=0.473113 (66232/139992, GnomAD) (+ 21 more)
A=0.48883 (38472/78702, PAGE_STUDY)
G=0.35225 (9954/28258, 14KJPN)
G=0.35334 (5922/16760, 8.3KJPN)
A=0.4927 (3155/6404, 1000G_30x)
A=0.4954 (2481/5008, 1000G)
G=0.3342 (1497/4480, Estonian)
G=0.4030 (1553/3854, ALSPAC)
G=0.3981 (1476/3708, TWINSUK)
G=0.3352 (982/2930, KOREAN)
A=0.4984 (943/1892, HapMap)
G=0.3384 (620/1832, Korea1K)
G=0.378 (377/998, GoNL)
G=0.364 (285/782, PRJEB37584)
G=0.358 (224/626, Chileans)
G=0.475 (285/600, NorthernSweden)
A=0.320 (126/394, SGDP_PRJ)
G=0.417 (90/216, Qatari)
G=0.368 (78/212, Vietnamese)
G=0.36 (18/50, Ancient Sardinia)
G=0.42 (17/40, GENOME_DK)
A=0.37 (11/30, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CFAP43 : Intron 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 191706 A=0.585522 G=0.414478
European Sub 160962 A=0.597973 G=0.402027
African Sub 8838 A=0.3359 G=0.6641
African Others Sub 298 A=0.346 G=0.654
African American Sub 8540 A=0.3356 G=0.6644
Asian Sub 6356 A=0.6076 G=0.3924
East Asian Sub 4504 A=0.6481 G=0.3519
Other Asian Sub 1852 A=0.5092 G=0.4908
Latin American 1 Sub 608 A=0.530 G=0.470
Latin American 2 Sub 3170 A=0.6656 G=0.3344
South Asian Sub 294 A=0.493 G=0.507
Other Sub 11478 A=0.57405 G=0.42595


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 A=0.522082 G=0.477918
Allele Frequency Aggregator Total Global 191490 A=0.585524 G=0.414476
Allele Frequency Aggregator European Sub 160782 A=0.597977 G=0.402023
Allele Frequency Aggregator Other Sub 11456 A=0.57394 G=0.42606
Allele Frequency Aggregator African Sub 8824 A=0.3359 G=0.6641
Allele Frequency Aggregator Asian Sub 6356 A=0.6076 G=0.3924
Allele Frequency Aggregator Latin American 2 Sub 3170 A=0.6656 G=0.3344
Allele Frequency Aggregator Latin American 1 Sub 608 A=0.530 G=0.470
Allele Frequency Aggregator South Asian Sub 294 A=0.493 G=0.507
gnomAD - Genomes Global Study-wide 139992 A=0.526887 G=0.473113
gnomAD - Genomes European Sub 75826 A=0.60717 G=0.39283
gnomAD - Genomes African Sub 41924 A=0.35097 G=0.64903
gnomAD - Genomes American Sub 13646 A=0.58493 G=0.41507
gnomAD - Genomes Ashkenazi Jewish Sub 3322 A=0.5858 G=0.4142
gnomAD - Genomes East Asian Sub 3124 A=0.6069 G=0.3931
gnomAD - Genomes Other Sub 2150 A=0.5502 G=0.4498
The PAGE Study Global Study-wide 78702 A=0.48883 G=0.51117
The PAGE Study AfricanAmerican Sub 32516 A=0.35026 G=0.64974
The PAGE Study Mexican Sub 10810 A=0.68011 G=0.31989
The PAGE Study Asian Sub 8318 A=0.6315 G=0.3685
The PAGE Study PuertoRican Sub 7918 A=0.4997 G=0.5003
The PAGE Study NativeHawaiian Sub 4534 A=0.5121 G=0.4879
The PAGE Study Cuban Sub 4230 A=0.5468 G=0.4532
The PAGE Study Dominican Sub 3828 A=0.4812 G=0.5188
The PAGE Study CentralAmerican Sub 2450 A=0.6392 G=0.3608
The PAGE Study SouthAmerican Sub 1982 A=0.6438 G=0.3562
The PAGE Study NativeAmerican Sub 1260 A=0.6222 G=0.3778
The PAGE Study SouthAsian Sub 856 A=0.488 G=0.512
14KJPN JAPANESE Study-wide 28258 A=0.64775 G=0.35225
8.3KJPN JAPANESE Study-wide 16760 A=0.64666 G=0.35334
1000Genomes_30x Global Study-wide 6404 A=0.4927 G=0.5073
1000Genomes_30x African Sub 1786 A=0.3024 G=0.6976
1000Genomes_30x Europe Sub 1266 A=0.5656 G=0.4344
1000Genomes_30x South Asian Sub 1202 A=0.4692 G=0.5308
1000Genomes_30x East Asian Sub 1170 A=0.6017 G=0.3983
1000Genomes_30x American Sub 980 A=0.644 G=0.356
1000Genomes Global Study-wide 5008 A=0.4954 G=0.5046
1000Genomes African Sub 1322 A=0.3041 G=0.6959
1000Genomes East Asian Sub 1008 A=0.5972 G=0.4028
1000Genomes Europe Sub 1006 A=0.5676 G=0.4324
1000Genomes South Asian Sub 978 A=0.472 G=0.528
1000Genomes American Sub 694 A=0.640 G=0.360
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.6658 G=0.3342
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.5970 G=0.4030
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.6019 G=0.3981
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.6648 G=0.3352
HapMap Global Study-wide 1892 A=0.4984 G=0.5016
HapMap American Sub 770 A=0.551 G=0.449
HapMap African Sub 692 A=0.386 G=0.614
HapMap Asian Sub 254 A=0.634 G=0.366
HapMap Europe Sub 176 A=0.517 G=0.483
Korean Genome Project KOREAN Study-wide 1832 A=0.6616 G=0.3384
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.622 G=0.378
CNV burdens in cranial meningiomas Global Study-wide 782 A=0.636 G=0.364
CNV burdens in cranial meningiomas CRM Sub 782 A=0.636 G=0.364
Chileans Chilean Study-wide 626 A=0.642 G=0.358
Northern Sweden ACPOP Study-wide 600 A=0.525 G=0.475
SGDP_PRJ Global Study-wide 394 A=0.320 G=0.680
Qatari Global Study-wide 216 A=0.583 G=0.417
A Vietnamese Genetic Variation Database Global Study-wide 212 A=0.632 G=0.368
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 50 A=0.64 G=0.36
The Danish reference pan genome Danish Study-wide 40 A=0.57 G=0.42
Siberian Global Study-wide 30 A=0.37 G=0.63
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 10 NC_000010.11:g.104206646A>G
GRCh37.p13 chr 10 NC_000010.10:g.105966404A>G
CFAP43 RefSeqGene NG_051581.1:g.30732T>C
Gene: CFAP43, cilia and flagella associated protein 43 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
CFAP43 transcript NM_025145.7:c.896-616T>C 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 A= G
GRCh38.p14 chr 10 NC_000010.11:g.104206646= NC_000010.11:g.104206646A>G
GRCh37.p13 chr 10 NC_000010.10:g.105966404= NC_000010.10:g.105966404A>G
CFAP43 RefSeqGene NG_051581.1:g.30732= NG_051581.1:g.30732T>C
CFAP43 transcript NM_025145.5:c.896-616= NM_025145.5:c.896-616T>C
CFAP43 transcript NM_025145.7:c.896-616= NM_025145.7:c.896-616T>C
CFAP43 transcript variant X3 XM_005270171.1:c.896-613= XM_005270171.1:c.896-613T>C
WDR96 transcript variant X2 XM_005270172.1:c.896-613= XM_005270172.1:c.896-613T>C
WDR96 transcript variant X3 XM_005270173.1:c.896-613= XM_005270173.1:c.896-613T>C
WDR96 transcript variant X4 XM_005270174.1:c.896-613= XM_005270174.1:c.896-613T>C
WDR96 transcript variant X5 XM_005270175.1:c.896-613= XM_005270175.1:c.896-613T>C
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#.

121 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss686148 Aug 11, 2000 (83)
2 KWOK ss958409 Oct 04, 2000 (86)
3 KWOK ss959842 Oct 04, 2000 (86)
4 KWOK ss1063240 Oct 04, 2000 (86)
5 KWOK ss1885498 Oct 18, 2000 (87)
6 KWOK ss1885831 Oct 18, 2000 (87)
7 KWOK ss1886365 Oct 18, 2000 (87)
8 TSC-CSHL ss2766646 Jan 22, 2001 (92)
9 WI_SSAHASNP ss12085803 Jul 11, 2003 (116)
10 SC_SNP ss15883299 Feb 27, 2004 (120)
11 SSAHASNP ss20712081 Apr 05, 2004 (121)
12 PERLEGEN ss24502629 Sep 20, 2004 (123)
13 ILLUMINA ss65718949 Oct 15, 2006 (127)
14 AFFY ss66046055 Nov 30, 2006 (127)
15 CSHL-HAPMAP ss68382144 Jan 12, 2007 (127)
16 PERLEGEN ss69089810 May 17, 2007 (127)
17 ILLUMINA ss74964596 Dec 06, 2007 (129)
18 AFFY ss75945563 Dec 08, 2007 (130)
19 KRIBB_YJKIM ss81424702 Dec 15, 2007 (130)
20 HGSV ss83902562 Dec 15, 2007 (130)
21 BCMHGSC_JDW ss88339096 Mar 23, 2008 (129)
22 HUMANGENOME_JCVI ss97581242 Feb 05, 2009 (130)
23 BGI ss102908458 Dec 01, 2009 (131)
24 1000GENOMES ss109712295 Jan 24, 2009 (130)
25 1000GENOMES ss113747793 Jan 25, 2009 (130)
26 ILLUMINA-UK ss119294078 Feb 15, 2009 (130)
27 ENSEMBL ss132055746 Dec 01, 2009 (131)
28 ENSEMBL ss138829330 Dec 01, 2009 (131)
29 AFFY ss169494289 Jul 04, 2010 (132)
30 COMPLETE_GENOMICS ss170977055 Jul 04, 2010 (132)
31 ILLUMINA ss173910883 Jul 04, 2010 (132)
32 COMPLETE_GENOMICS ss174731396 Jul 04, 2010 (132)
33 BUSHMAN ss201957332 Jul 04, 2010 (132)
34 BCM-HGSC-SUB ss207147353 Jul 04, 2010 (132)
35 1000GENOMES ss224913114 Jul 14, 2010 (132)
36 1000GENOMES ss235314858 Jul 15, 2010 (132)
37 1000GENOMES ss241993871 Jul 15, 2010 (132)
38 BL ss254588343 May 09, 2011 (134)
39 GMI ss280754431 May 04, 2012 (137)
40 PJP ss290921644 May 09, 2011 (134)
41 EXOME_CHIP ss491440384 May 04, 2012 (137)
42 ILLUMINA ss537306255 Sep 08, 2015 (146)
43 TISHKOFF ss562178077 Apr 25, 2013 (138)
44 SSMP ss657271718 Apr 25, 2013 (138)
45 ILLUMINA ss783359074 Aug 21, 2014 (142)
46 EVA-GONL ss987869468 Aug 21, 2014 (142)
47 JMKIDD_LAB ss1077258285 Aug 21, 2014 (142)
48 1000GENOMES ss1338871274 Aug 21, 2014 (142)
49 DDI ss1426429552 Apr 01, 2015 (144)
50 EVA_GENOME_DK ss1575328947 Apr 01, 2015 (144)
51 EVA_DECODE ss1597544884 Apr 01, 2015 (144)
52 EVA_UK10K_ALSPAC ss1625329620 Apr 01, 2015 (144)
53 EVA_UK10K_TWINSUK ss1668323653 Apr 01, 2015 (144)
54 EVA_SVP ss1713207508 Apr 01, 2015 (144)
55 ILLUMINA ss1751944637 Sep 08, 2015 (146)
56 HAMMER_LAB ss1806547054 Sep 08, 2015 (146)
57 ILLUMINA ss1917851425 Feb 12, 2016 (147)
58 WEILL_CORNELL_DGM ss1931231952 Feb 12, 2016 (147)
59 ILLUMINA ss1946292392 Feb 12, 2016 (147)
60 ILLUMINA ss1959291507 Feb 12, 2016 (147)
61 GENOMED ss1967212902 Jul 19, 2016 (147)
62 JJLAB ss2026346759 Sep 14, 2016 (149)
63 USC_VALOUEV ss2154626103 Nov 08, 2017 (151)
64 HUMAN_LONGEVITY ss2177673505 Dec 20, 2016 (150)
65 SYSTEMSBIOZJU ss2627641447 Nov 08, 2017 (151)
66 ILLUMINA ss2632756363 Nov 08, 2017 (151)
67 ILLUMINA ss2635018576 Nov 08, 2017 (151)
68 GRF ss2698880026 Nov 08, 2017 (151)
69 GNOMAD ss2892860730 Nov 08, 2017 (151)
70 AFFY ss2984922693 Nov 08, 2017 (151)
71 AFFY ss2985569642 Nov 08, 2017 (151)
72 SWEGEN ss3007071323 Nov 08, 2017 (151)
73 ILLUMINA ss3021271662 Nov 08, 2017 (151)
74 BIOINF_KMB_FNS_UNIBA ss3026963126 Nov 08, 2017 (151)
75 CSHL ss3349289097 Nov 08, 2017 (151)
76 ILLUMINA ss3626524590 Oct 12, 2018 (152)
77 ILLUMINA ss3634422003 Oct 12, 2018 (152)
78 ILLUMINA ss3637871577 Oct 12, 2018 (152)
79 ILLUMINA ss3640129344 Oct 12, 2018 (152)
80 ILLUMINA ss3642873219 Oct 12, 2018 (152)
81 ILLUMINA ss3644545143 Oct 12, 2018 (152)
82 URBANLAB ss3649455348 Oct 12, 2018 (152)
83 ILLUMINA ss3651630783 Oct 12, 2018 (152)
84 ILLUMINA ss3653693582 Oct 12, 2018 (152)
85 EGCUT_WGS ss3674482702 Jul 13, 2019 (153)
86 EVA_DECODE ss3690589720 Jul 13, 2019 (153)
87 ILLUMINA ss3725185574 Jul 13, 2019 (153)
88 ACPOP ss3737638642 Jul 13, 2019 (153)
89 ILLUMINA ss3744371642 Jul 13, 2019 (153)
90 ILLUMINA ss3744722971 Jul 13, 2019 (153)
91 EVA ss3748544198 Jul 13, 2019 (153)
92 PAGE_CC ss3771580744 Jul 13, 2019 (153)
93 ILLUMINA ss3772223256 Jul 13, 2019 (153)
94 PACBIO ss3786774625 Jul 13, 2019 (153)
95 PACBIO ss3791938662 Jul 13, 2019 (153)
96 PACBIO ss3796820767 Jul 13, 2019 (153)
97 KHV_HUMAN_GENOMES ss3813904920 Jul 13, 2019 (153)
98 EVA ss3832307973 Apr 26, 2020 (154)
99 SGDP_PRJ ss3874954971 Apr 26, 2020 (154)
100 KRGDB ss3923111455 Apr 26, 2020 (154)
101 KOGIC ss3968589953 Apr 26, 2020 (154)
102 EVA ss3984640202 Apr 27, 2021 (155)
103 EVA ss3985497048 Apr 27, 2021 (155)
104 EVA ss4017505312 Apr 27, 2021 (155)
105 TOPMED ss4864852387 Apr 27, 2021 (155)
106 TOMMO_GENOMICS ss5199267886 Apr 27, 2021 (155)
107 1000G_HIGH_COVERAGE ss5285304454 Oct 16, 2022 (156)
108 EVA ss5315499132 Oct 16, 2022 (156)
109 EVA ss5395724731 Oct 16, 2022 (156)
110 HUGCELL_USP ss5480742655 Oct 16, 2022 (156)
111 EVA ss5510151116 Oct 16, 2022 (156)
112 1000G_HIGH_COVERAGE ss5579891266 Oct 16, 2022 (156)
113 SANFORD_IMAGENETICS ss5624257421 Oct 16, 2022 (156)
114 SANFORD_IMAGENETICS ss5650002825 Oct 16, 2022 (156)
115 TOMMO_GENOMICS ss5745578729 Oct 16, 2022 (156)
116 YY_MCH ss5811844992 Oct 16, 2022 (156)
117 EVA ss5824893862 Oct 16, 2022 (156)
118 EVA ss5847608813 Oct 16, 2022 (156)
119 EVA ss5849721060 Oct 16, 2022 (156)
120 EVA ss5880335024 Oct 16, 2022 (156)
121 EVA ss5941296836 Oct 16, 2022 (156)
122 1000Genomes NC_000010.10 - 105966404 Oct 12, 2018 (152)
123 1000Genomes_30x NC_000010.11 - 104206646 Oct 16, 2022 (156)
124 The Avon Longitudinal Study of Parents and Children NC_000010.10 - 105966404 Oct 12, 2018 (152)
125 Chileans NC_000010.10 - 105966404 Apr 26, 2020 (154)
126 Genetic variation in the Estonian population NC_000010.10 - 105966404 Oct 12, 2018 (152)
127 The Danish reference pan genome NC_000010.10 - 105966404 Apr 26, 2020 (154)
128 gnomAD - Genomes NC_000010.11 - 104206646 Apr 27, 2021 (155)
129 Genome of the Netherlands Release 5 NC_000010.10 - 105966404 Apr 26, 2020 (154)
130 HapMap NC_000010.11 - 104206646 Apr 26, 2020 (154)
131 KOREAN population from KRGDB NC_000010.10 - 105966404 Apr 26, 2020 (154)
132 Korean Genome Project NC_000010.11 - 104206646 Apr 26, 2020 (154)
133 Northern Sweden NC_000010.10 - 105966404 Jul 13, 2019 (153)
134 The PAGE Study NC_000010.11 - 104206646 Jul 13, 2019 (153)
135 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000010.10 - 105966404 Apr 27, 2021 (155)
136 CNV burdens in cranial meningiomas NC_000010.10 - 105966404 Apr 27, 2021 (155)
137 Qatari NC_000010.10 - 105966404 Apr 26, 2020 (154)
138 SGDP_PRJ NC_000010.10 - 105966404 Apr 26, 2020 (154)
139 Siberian NC_000010.10 - 105966404 Apr 26, 2020 (154)
140 8.3KJPN NC_000010.10 - 105966404 Apr 27, 2021 (155)
141 14KJPN NC_000010.11 - 104206646 Oct 16, 2022 (156)
142 TopMed NC_000010.11 - 104206646 Apr 27, 2021 (155)
143 UK 10K study - Twins NC_000010.10 - 105966404 Oct 12, 2018 (152)
144 A Vietnamese Genetic Variation Database NC_000010.10 - 105966404 Jul 13, 2019 (153)
145 ALFA NC_000010.11 - 104206646 Apr 27, 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)
rs17824623 Oct 08, 2004 (123)
rs56473449 May 24, 2008 (130)
rs58815707 Feb 26, 2009 (130)
rs58823292 May 24, 2008 (130)
rs386597813 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss83902562 NC_000010.8:105956393:A:G NC_000010.11:104206645:A:G (self)
ss66046055, ss75945563, ss88339096, ss109712295, ss113747793, ss119294078, ss169494289, ss170977055, ss174731396, ss201957332, ss207147353, ss254588343, ss280754431, ss290921644, ss1597544884, ss1713207508, ss2635018576, ss3642873219 NC_000010.9:105956393:A:G NC_000010.11:104206645:A:G (self)
51311703, 28493306, 59849, 20220950, 2307193, 12702007, 30288849, 10923507, 722975, 189672, 13273882, 26971951, 7142457, 57237193, 28493306, 6324085, ss224913114, ss235314858, ss241993871, ss491440384, ss537306255, ss562178077, ss657271718, ss783359074, ss987869468, ss1077258285, ss1338871274, ss1426429552, ss1575328947, ss1625329620, ss1668323653, ss1751944637, ss1806547054, ss1917851425, ss1931231952, ss1946292392, ss1959291507, ss1967212902, ss2026346759, ss2154626103, ss2627641447, ss2632756363, ss2698880026, ss2892860730, ss2984922693, ss2985569642, ss3007071323, ss3021271662, ss3349289097, ss3626524590, ss3634422003, ss3637871577, ss3640129344, ss3644545143, ss3651630783, ss3653693582, ss3674482702, ss3737638642, ss3744371642, ss3744722971, ss3748544198, ss3772223256, ss3786774625, ss3791938662, ss3796820767, ss3832307973, ss3874954971, ss3923111455, ss3984640202, ss3985497048, ss4017505312, ss5199267886, ss5315499132, ss5395724731, ss5510151116, ss5624257421, ss5650002825, ss5824893862, ss5847608813, ss5941296836 NC_000010.10:105966403:A:G NC_000010.11:104206645:A:G (self)
67417201, 362618088, 480191, 24967954, 802213, 79415833, 80398042, 12399685966, ss2177673505, ss3026963126, ss3649455348, ss3690589720, ss3725185574, ss3771580744, ss3813904920, ss3968589953, ss4864852387, ss5285304454, ss5480742655, ss5579891266, ss5745578729, ss5811844992, ss5849721060, ss5880335024 NC_000010.11:104206645:A:G NC_000010.11:104206645:A:G (self)
ss12085803 NT_030059.10:24404961:A:G NC_000010.11:104206645:A:G (self)
ss15883299, ss20712081 NT_030059.11:24714929:A:G NC_000010.11:104206645:A:G (self)
ss686148, ss958409, ss959842, ss1063240, ss1885498, ss1885831, ss1886365, ss2766646, ss24502629, ss65718949, ss68382144, ss69089810, ss74964596, ss81424702, ss97581242, ss102908458, ss132055746, ss138829330, ss173910883 NT_030059.13:56770867:A:G NC_000010.11:104206645:A:G (self)
Help

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

1 citation for rs515910
PMID Title Author Year Journal
19384554 Genome-wide association studies in ADHD. Franke B et al. 2009 Human genetics
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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
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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.

Software version is: 2.0.1.post761+d5e8e07