Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs7175404

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr15:93493459 (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=0.279705 (74035/264690, TOPMED)
G=0.179886 (34323/190804, ALFA)
G=0.259561 (36350/140044, GnomAD) (+ 22 more)
G=0.38441 (30251/78694, PAGE_STUDY)
G=0.43177 (12201/28258, 14KJPN)
G=0.43693 (7323/16760, 8.3KJPN)
G=0.3884 (2487/6404, 1000G_30x)
G=0.3866 (1936/5008, 1000G)
G=0.1257 (563/4480, Estonian)
G=0.1539 (593/3854, ALSPAC)
G=0.1335 (495/3708, TWINSUK)
G=0.4232 (1240/2930, KOREAN)
G=0.3556 (741/2084, HGDP_Stanford)
G=0.3916 (741/1892, HapMap)
G=0.4083 (748/1832, Korea1K)
G=0.156 (156/998, GoNL)
G=0.439 (345/786, PRJEB37584)
G=0.332 (208/626, Chileans)
G=0.128 (77/600, NorthernSweden)
A=0.313 (102/326, SGDP_PRJ)
G=0.306 (66/216, Qatari)
G=0.467 (100/214, Vietnamese)
G=0.05 (2/44, Ancient Sardinia)
G=0.07 (3/40, GENOME_DK)
A=0.35 (9/26, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
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 191020 A=0.820165 G=0.179835
European Sub 160312 A=0.855226 G=0.144774
African Sub 8836 A=0.5470 G=0.4530
African Others Sub 298 A=0.503 G=0.497
African American Sub 8538 A=0.5485 G=0.4515
Asian Sub 6350 A=0.5483 G=0.4517
East Asian Sub 4500 A=0.5578 G=0.4422
Other Asian Sub 1850 A=0.5254 G=0.4746
Latin American 1 Sub 610 A=0.741 G=0.259
Latin American 2 Sub 3170 A=0.6991 G=0.3009
South Asian Sub 294 A=0.592 G=0.408
Other Sub 11448 A=0.73445 G=0.26555


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=0.720295 G=0.279705
Allele Frequency Aggregator Total Global 190804 A=0.820114 G=0.179886
Allele Frequency Aggregator European Sub 160132 A=0.855194 G=0.144806
Allele Frequency Aggregator Other Sub 11426 A=0.73412 G=0.26588
Allele Frequency Aggregator African Sub 8822 A=0.5469 G=0.4531
Allele Frequency Aggregator Asian Sub 6350 A=0.5483 G=0.4517
Allele Frequency Aggregator Latin American 2 Sub 3170 A=0.6991 G=0.3009
Allele Frequency Aggregator Latin American 1 Sub 610 A=0.741 G=0.259
Allele Frequency Aggregator South Asian Sub 294 A=0.592 G=0.408
gnomAD - Genomes Global Study-wide 140044 A=0.740439 G=0.259561
gnomAD - Genomes European Sub 75886 A=0.85038 G=0.14962
gnomAD - Genomes African Sub 41936 A=0.55289 G=0.44711
gnomAD - Genomes American Sub 13628 A=0.72512 G=0.27488
gnomAD - Genomes Ashkenazi Jewish Sub 3320 A=0.8590 G=0.1410
gnomAD - Genomes East Asian Sub 3124 A=0.5439 G=0.4561
gnomAD - Genomes Other Sub 2150 A=0.7177 G=0.2823
The PAGE Study Global Study-wide 78694 A=0.61559 G=0.38441
The PAGE Study AfricanAmerican Sub 32516 A=0.55797 G=0.44203
The PAGE Study Mexican Sub 10808 A=0.69671 G=0.30329
The PAGE Study Asian Sub 8318 A=0.5471 G=0.4529
The PAGE Study PuertoRican Sub 7916 A=0.7188 G=0.2812
The PAGE Study NativeHawaiian Sub 4532 A=0.5428 G=0.4572
The PAGE Study Cuban Sub 4230 A=0.7494 G=0.2506
The PAGE Study Dominican Sub 3828 A=0.6758 G=0.3242
The PAGE Study CentralAmerican Sub 2450 A=0.6392 G=0.3608
The PAGE Study SouthAmerican Sub 1982 A=0.6473 G=0.3527
The PAGE Study NativeAmerican Sub 1258 A=0.7742 G=0.2258
The PAGE Study SouthAsian Sub 856 A=0.571 G=0.429
14KJPN JAPANESE Study-wide 28258 A=0.56823 G=0.43177
8.3KJPN JAPANESE Study-wide 16760 A=0.56307 G=0.43693
1000Genomes_30x Global Study-wide 6404 A=0.6116 G=0.3884
1000Genomes_30x African Sub 1786 A=0.5045 G=0.4955
1000Genomes_30x Europe Sub 1266 A=0.8483 G=0.1517
1000Genomes_30x South Asian Sub 1202 A=0.5657 G=0.4343
1000Genomes_30x East Asian Sub 1170 A=0.5274 G=0.4726
1000Genomes_30x American Sub 980 A=0.658 G=0.342
1000Genomes Global Study-wide 5008 A=0.6134 G=0.3866
1000Genomes African Sub 1322 A=0.5121 G=0.4879
1000Genomes East Asian Sub 1008 A=0.5258 G=0.4742
1000Genomes Europe Sub 1006 A=0.8419 G=0.1581
1000Genomes South Asian Sub 978 A=0.571 G=0.429
1000Genomes American Sub 694 A=0.663 G=0.337
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.8743 G=0.1257
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.8461 G=0.1539
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.8665 G=0.1335
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.5768 G=0.4232
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.6444 G=0.3556
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.538 G=0.462
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.616 G=0.384
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.709 G=0.291
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.809 G=0.191
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.508 G=0.492
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.681 G=0.319
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.81 G=0.19
HapMap Global Study-wide 1892 A=0.6084 G=0.3916
HapMap American Sub 770 A=0.644 G=0.356
HapMap African Sub 692 A=0.530 G=0.470
HapMap Asian Sub 254 A=0.524 G=0.476
HapMap Europe Sub 176 A=0.881 G=0.119
Korean Genome Project KOREAN Study-wide 1832 A=0.5917 G=0.4083
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.844 G=0.156
CNV burdens in cranial meningiomas Global Study-wide 786 A=0.561 G=0.439
CNV burdens in cranial meningiomas CRM Sub 786 A=0.561 G=0.439
Chileans Chilean Study-wide 626 A=0.668 G=0.332
Northern Sweden ACPOP Study-wide 600 A=0.872 G=0.128
SGDP_PRJ Global Study-wide 326 A=0.313 G=0.687
Qatari Global Study-wide 216 A=0.694 G=0.306
A Vietnamese Genetic Variation Database Global Study-wide 214 A=0.533 G=0.467
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 44 A=0.95 G=0.05
The Danish reference pan genome Danish Study-wide 40 A=0.93 G=0.07
Siberian Global Study-wide 26 A=0.35 G=0.65
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 15 NC_000015.10:g.93493459A>G
GRCh37.p13 chr 15 NC_000015.9:g.94036688A>G
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 15 NC_000015.10:g.93493459= NC_000015.10:g.93493459A>G
GRCh37.p13 chr 15 NC_000015.9:g.94036688= NC_000015.9:g.94036688A>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#.

104 SubSNP, 25 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss10787820 Jul 11, 2003 (116)
2 PERLEGEN ss24183413 Sep 20, 2004 (123)
3 AFFY ss66116618 Dec 01, 2006 (127)
4 ILLUMINA ss67926104 Dec 01, 2006 (127)
5 ILLUMINA ss71511942 May 17, 2007 (127)
6 ILLUMINA ss75363119 Dec 07, 2007 (129)
7 AFFY ss76104304 Dec 08, 2007 (130)
8 KRIBB_YJKIM ss82399060 Dec 15, 2007 (130)
9 HGSV ss84038510 Dec 15, 2007 (130)
10 BCMHGSC_JDW ss90258275 Mar 24, 2008 (129)
11 ILLUMINA-UK ss118336026 Feb 14, 2009 (130)
12 ENSEMBL ss136500460 Dec 01, 2009 (131)
13 GMI ss156880952 Dec 01, 2009 (131)
14 AFFY ss172519615 Jul 04, 2010 (132)
15 ILLUMINA ss174274803 Jul 04, 2010 (132)
16 BCM-HGSC-SUB ss207296117 Jul 04, 2010 (132)
17 1000GENOMES ss211653983 Jul 14, 2010 (132)
18 1000GENOMES ss227046451 Jul 14, 2010 (132)
19 1000GENOMES ss236886175 Jul 15, 2010 (132)
20 1000GENOMES ss243253195 Jul 15, 2010 (132)
21 GMI ss282370170 May 04, 2012 (137)
22 GMI ss287005218 Apr 25, 2013 (138)
23 PJP ss291778993 May 09, 2011 (134)
24 EXOME_CHIP ss491499983 May 04, 2012 (137)
25 ILLUMINA ss537445448 Sep 08, 2015 (146)
26 TISHKOFF ss564663161 Apr 25, 2013 (138)
27 SSMP ss660406244 Apr 25, 2013 (138)
28 ILLUMINA ss780686370 Sep 08, 2015 (146)
29 ILLUMINA ss783359889 Sep 08, 2015 (146)
30 EVA-GONL ss992099570 Aug 21, 2014 (142)
31 JMKIDD_LAB ss1080352929 Aug 21, 2014 (142)
32 1000GENOMES ss1354678588 Aug 21, 2014 (142)
33 DDI ss1427721681 Apr 01, 2015 (144)
34 EVA_GENOME_DK ss1577759554 Apr 01, 2015 (144)
35 EVA_UK10K_ALSPAC ss1633647277 Apr 01, 2015 (144)
36 EVA_UK10K_TWINSUK ss1676641310 Apr 01, 2015 (144)
37 EVA_DECODE ss1696129623 Apr 01, 2015 (144)
38 EVA_SVP ss1713512943 Apr 01, 2015 (144)
39 ILLUMINA ss1752178606 Sep 08, 2015 (146)
40 HAMMER_LAB ss1808337288 Sep 08, 2015 (146)
41 ILLUMINA ss1917901153 Feb 12, 2016 (147)
42 WEILL_CORNELL_DGM ss1935502597 Feb 12, 2016 (147)
43 ILLUMINA ss1946403052 Feb 12, 2016 (147)
44 ILLUMINA ss1959639848 Feb 12, 2016 (147)
45 GENOMED ss1968178661 Jul 19, 2016 (147)
46 JJLAB ss2028535618 Sep 14, 2016 (149)
47 USC_VALOUEV ss2156944944 Nov 08, 2017 (151)
48 HUMAN_LONGEVITY ss2209234979 Dec 20, 2016 (150)
49 SYSTEMSBIOZJU ss2628763027 Nov 08, 2017 (151)
50 GRF ss2701433167 Nov 08, 2017 (151)
51 GNOMAD ss2938374056 Nov 08, 2017 (151)
52 AFFY ss2985052271 Nov 08, 2017 (151)
53 AFFY ss2985692263 Nov 08, 2017 (151)
54 SWEGEN ss3013779596 Nov 08, 2017 (151)
55 ILLUMINA ss3021663417 Nov 08, 2017 (151)
56 BIOINF_KMB_FNS_UNIBA ss3028092225 Nov 08, 2017 (151)
57 CSHL ss3351251219 Nov 08, 2017 (151)
58 ILLUMINA ss3627435057 Oct 12, 2018 (152)
59 ILLUMINA ss3627435058 Oct 12, 2018 (152)
60 ILLUMINA ss3634622280 Oct 12, 2018 (152)
61 ILLUMINA ss3638103632 Oct 12, 2018 (152)
62 ILLUMINA ss3640329600 Oct 12, 2018 (152)
63 ILLUMINA ss3643086489 Oct 12, 2018 (152)
64 ILLUMINA ss3644656169 Oct 12, 2018 (152)
65 ILLUMINA ss3652066441 Oct 12, 2018 (152)
66 ILLUMINA ss3653824349 Oct 12, 2018 (152)
67 EGCUT_WGS ss3680909731 Jul 13, 2019 (153)
68 EVA_DECODE ss3698493047 Jul 13, 2019 (153)
69 ILLUMINA ss3725526898 Jul 13, 2019 (153)
70 ACPOP ss3741184142 Jul 13, 2019 (153)
71 ILLUMINA ss3744425258 Jul 13, 2019 (153)
72 ILLUMINA ss3744922799 Jul 13, 2019 (153)
73 EVA ss3753466219 Jul 13, 2019 (153)
74 PAGE_CC ss3771852171 Jul 13, 2019 (153)
75 ILLUMINA ss3772421277 Jul 13, 2019 (153)
76 PACBIO ss3787932069 Jul 13, 2019 (153)
77 PACBIO ss3792930613 Jul 13, 2019 (153)
78 PACBIO ss3797815267 Jul 13, 2019 (153)
79 KHV_HUMAN_GENOMES ss3818767894 Jul 13, 2019 (153)
80 EVA ss3834385242 Apr 27, 2020 (154)
81 HGDP ss3847533669 Apr 27, 2020 (154)
82 SGDP_PRJ ss3883559679 Apr 27, 2020 (154)
83 KRGDB ss3932815171 Apr 27, 2020 (154)
84 KOGIC ss3976773168 Apr 27, 2020 (154)
85 EVA ss3984706531 Apr 26, 2021 (155)
86 EVA ss3985735606 Apr 26, 2021 (155)
87 EVA ss4017717844 Apr 26, 2021 (155)
88 TOPMED ss5001983366 Apr 26, 2021 (155)
89 TOMMO_GENOMICS ss5217617237 Apr 26, 2021 (155)
90 1000G_HIGH_COVERAGE ss5299513593 Oct 16, 2022 (156)
91 EVA ss5315808443 Oct 16, 2022 (156)
92 EVA ss5421190536 Oct 16, 2022 (156)
93 HUGCELL_USP ss5493119234 Oct 16, 2022 (156)
94 EVA ss5511524796 Oct 16, 2022 (156)
95 1000G_HIGH_COVERAGE ss5601446894 Oct 16, 2022 (156)
96 SANFORD_IMAGENETICS ss5624369305 Oct 16, 2022 (156)
97 SANFORD_IMAGENETICS ss5658112593 Oct 16, 2022 (156)
98 TOMMO_GENOMICS ss5771853723 Oct 16, 2022 (156)
99 YY_MCH ss5815603013 Oct 16, 2022 (156)
100 EVA ss5828615132 Oct 16, 2022 (156)
101 EVA ss5847755436 Oct 16, 2022 (156)
102 EVA ss5851417548 Oct 16, 2022 (156)
103 EVA ss5877099373 Oct 16, 2022 (156)
104 EVA ss5949538017 Oct 16, 2022 (156)
105 1000Genomes NC_000015.9 - 94036688 Oct 12, 2018 (152)
106 1000Genomes_30x NC_000015.10 - 93493459 Oct 16, 2022 (156)
107 The Avon Longitudinal Study of Parents and Children NC_000015.9 - 94036688 Oct 12, 2018 (152)
108 Chileans NC_000015.9 - 94036688 Apr 27, 2020 (154)
109 Genetic variation in the Estonian population NC_000015.9 - 94036688 Oct 12, 2018 (152)
110 The Danish reference pan genome NC_000015.9 - 94036688 Apr 27, 2020 (154)
111 gnomAD - Genomes NC_000015.10 - 93493459 Apr 26, 2021 (155)
112 Genome of the Netherlands Release 5 NC_000015.9 - 94036688 Apr 27, 2020 (154)
113 HGDP-CEPH-db Supplement 1 NC_000015.8 - 91837692 Apr 27, 2020 (154)
114 HapMap NC_000015.10 - 93493459 Apr 27, 2020 (154)
115 KOREAN population from KRGDB NC_000015.9 - 94036688 Apr 27, 2020 (154)
116 Korean Genome Project NC_000015.10 - 93493459 Apr 27, 2020 (154)
117 Northern Sweden NC_000015.9 - 94036688 Jul 13, 2019 (153)
118 The PAGE Study NC_000015.10 - 93493459 Jul 13, 2019 (153)
119 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000015.9 - 94036688 Apr 26, 2021 (155)
120 CNV burdens in cranial meningiomas NC_000015.9 - 94036688 Apr 26, 2021 (155)
121 Qatari NC_000015.9 - 94036688 Apr 27, 2020 (154)
122 SGDP_PRJ NC_000015.9 - 94036688 Apr 27, 2020 (154)
123 Siberian NC_000015.9 - 94036688 Apr 27, 2020 (154)
124 8.3KJPN NC_000015.9 - 94036688 Apr 26, 2021 (155)
125 14KJPN NC_000015.10 - 93493459 Oct 16, 2022 (156)
126 TopMed NC_000015.10 - 93493459 Apr 26, 2021 (155)
127 UK 10K study - Twins NC_000015.9 - 94036688 Oct 12, 2018 (152)
128 A Vietnamese Genetic Variation Database NC_000015.9 - 94036688 Jul 13, 2019 (153)
129 ALFA NC_000015.10 - 93493459 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)
rs17708421 Oct 08, 2004 (123)
rs56640139 May 25, 2008 (130)
rs58862633 May 25, 2008 (130)
rs59287388 Feb 26, 2009 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
211561, ss84038510, ss90258275, ss118336026, ss207296117, ss211653983, ss282370170, ss287005218, ss291778993, ss1696129623, ss1713512943, ss3643086489, ss3847533669 NC_000015.8:91837691:A:G NC_000015.10:93493458:A:G (self)
67793410, 37650486, 159894, 26647979, 3978371, 16798325, 39992565, 14469007, 961533, 256059, 17544519, 35576659, 9461298, 75586544, 37650486, 8368854, ss227046451, ss236886175, ss243253195, ss491499983, ss537445448, ss564663161, ss660406244, ss780686370, ss783359889, ss992099570, ss1080352929, ss1354678588, ss1427721681, ss1577759554, ss1633647277, ss1676641310, ss1752178606, ss1808337288, ss1917901153, ss1935502597, ss1946403052, ss1959639848, ss1968178661, ss2028535618, ss2156944944, ss2628763027, ss2701433167, ss2938374056, ss2985052271, ss2985692263, ss3013779596, ss3021663417, ss3351251219, ss3627435057, ss3627435058, ss3634622280, ss3638103632, ss3640329600, ss3644656169, ss3652066441, ss3653824349, ss3680909731, ss3741184142, ss3744425258, ss3744922799, ss3753466219, ss3772421277, ss3787932069, ss3792930613, ss3797815267, ss3834385242, ss3883559679, ss3932815171, ss3984706531, ss3985735606, ss4017717844, ss5217617237, ss5315808443, ss5421190536, ss5511524796, ss5624369305, ss5658112593, ss5828615132, ss5847755436, ss5949538017 NC_000015.9:94036687:A:G NC_000015.10:93493458:A:G (self)
88972829, 477919151, 1319719, 33151169, 1073640, 105690827, 217529026, 1713214564, ss2209234979, ss3028092225, ss3698493047, ss3725526898, ss3771852171, ss3818767894, ss3976773168, ss5001983366, ss5299513593, ss5493119234, ss5601446894, ss5771853723, ss5815603013, ss5851417548, ss5877099373 NC_000015.10:93493458:A:G NC_000015.10:93493458:A:G (self)
ss10787820 NT_010274.15:9002214:A:G NC_000015.10:93493458:A:G (self)
ss24183413, ss66116618, ss67926104, ss71511942, ss75363119, ss76104304, ss82399060, ss136500460, ss156880952, ss172519615, ss174274803 NT_010274.17:9002214:A:G NC_000015.10:93493458: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 rs7175404
PMID Title Author Year Journal
19384554 Genome-wide association studies in ADHD. Franke B et al. 2009 Human genetics
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