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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.

rs10938494

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr4:47561431 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.220821 (58449/264690, TOPMED)
A=0.220444 (54421/246870, ALFA)
A=0.215657 (30204/140056, GnomAD) (+ 21 more)
A=0.22215 (17482/78696, PAGE_STUDY)
A=0.21905 (6190/28258, 14KJPN)
A=0.22053 (3696/16760, 8.3KJPN)
A=0.2244 (1437/6404, 1000G_30x)
A=0.2234 (1119/5008, 1000G)
A=0.2114 (947/4480, Estonian)
A=0.2089 (805/3854, ALSPAC)
A=0.2222 (824/3708, TWINSUK)
A=0.2679 (785/2930, KOREAN)
A=0.2505 (522/2084, HGDP_Stanford)
A=0.2199 (412/1874, HapMap)
A=0.2434 (446/1832, Korea1K)
A=0.191 (191/998, GoNL)
A=0.276 (218/790, PRJEB37584)
A=0.173 (104/600, NorthernSweden)
A=0.292 (63/216, Qatari)
G=0.425 (91/214, SGDP_PRJ)
A=0.20 (8/40, GENOME_DK)
A=0.37 (14/38, Ancient Sardinia)
G=0.50 (11/22, Siberian)
A=0.50 (11/22, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ATP10D : 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 247084 G=0.779565 A=0.220435
European Sub 213422 G=0.781353 A=0.218647
African Sub 8568 G=0.8021 A=0.1979
African Others Sub 308 G=0.834 A=0.166
African American Sub 8260 G=0.8008 A=0.1992
Asian Sub 6398 G=0.7337 A=0.2663
East Asian Sub 4570 G=0.7295 A=0.2705
Other Asian Sub 1828 G=0.7440 A=0.2560
Latin American 1 Sub 550 G=0.724 A=0.276
Latin American 2 Sub 1568 G=0.7487 A=0.2513
South Asian Sub 5134 G=0.7900 A=0.2100
Other Sub 11444 G=0.75725 A=0.24275


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=0.779179 A=0.220821
Allele Frequency Aggregator Total Global 246870 G=0.779556 A=0.220444
Allele Frequency Aggregator European Sub 213244 G=0.781340 A=0.218660
Allele Frequency Aggregator Other Sub 11422 G=0.75740 A=0.24260
Allele Frequency Aggregator African Sub 8554 G=0.8020 A=0.1980
Allele Frequency Aggregator Asian Sub 6398 G=0.7337 A=0.2663
Allele Frequency Aggregator South Asian Sub 5134 G=0.7900 A=0.2100
Allele Frequency Aggregator Latin American 2 Sub 1568 G=0.7487 A=0.2513
Allele Frequency Aggregator Latin American 1 Sub 550 G=0.724 A=0.276
gnomAD - Genomes Global Study-wide 140056 G=0.784343 A=0.215657
gnomAD - Genomes European Sub 75860 G=0.78587 A=0.21413
gnomAD - Genomes African Sub 41970 G=0.80627 A=0.19373
gnomAD - Genomes American Sub 13636 G=0.74663 A=0.25337
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=0.7265 A=0.2735
gnomAD - Genomes East Asian Sub 3124 G=0.6972 A=0.3028
gnomAD - Genomes Other Sub 2142 G=0.7577 A=0.2423
The PAGE Study Global Study-wide 78696 G=0.77785 A=0.22215
The PAGE Study AfricanAmerican Sub 32514 G=0.80808 A=0.19192
The PAGE Study Mexican Sub 10808 G=0.75777 A=0.24223
The PAGE Study Asian Sub 8316 G=0.7462 A=0.2538
The PAGE Study PuertoRican Sub 7918 G=0.7770 A=0.2230
The PAGE Study NativeHawaiian Sub 4534 G=0.7417 A=0.2583
The PAGE Study Cuban Sub 4230 G=0.7532 A=0.2468
The PAGE Study Dominican Sub 3828 G=0.7774 A=0.2226
The PAGE Study CentralAmerican Sub 2450 G=0.7376 A=0.2624
The PAGE Study SouthAmerican Sub 1982 G=0.6937 A=0.3063
The PAGE Study NativeAmerican Sub 1260 G=0.7921 A=0.2079
The PAGE Study SouthAsian Sub 856 G=0.804 A=0.196
14KJPN JAPANESE Study-wide 28258 G=0.78095 A=0.21905
8.3KJPN JAPANESE Study-wide 16760 G=0.77947 A=0.22053
1000Genomes_30x Global Study-wide 6404 G=0.7756 A=0.2244
1000Genomes_30x African Sub 1786 G=0.8141 A=0.1859
1000Genomes_30x Europe Sub 1266 G=0.7820 A=0.2180
1000Genomes_30x South Asian Sub 1202 G=0.8286 A=0.1714
1000Genomes_30x East Asian Sub 1170 G=0.7171 A=0.2829
1000Genomes_30x American Sub 980 G=0.702 A=0.298
1000Genomes Global Study-wide 5008 G=0.7766 A=0.2234
1000Genomes African Sub 1322 G=0.8192 A=0.1808
1000Genomes East Asian Sub 1008 G=0.7133 A=0.2867
1000Genomes Europe Sub 1006 G=0.7863 A=0.2137
1000Genomes South Asian Sub 978 G=0.825 A=0.175
1000Genomes American Sub 694 G=0.705 A=0.295
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.7886 A=0.2114
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.7911 A=0.2089
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.7778 A=0.2222
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.7321 A=0.2679
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.7495 A=0.2505
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.757 A=0.243
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.751 A=0.249
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.709 A=0.291
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.750 A=0.250
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.843 A=0.157
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.630 A=0.370
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.93 A=0.07
HapMap Global Study-wide 1874 G=0.7801 A=0.2199
HapMap American Sub 764 G=0.764 A=0.236
HapMap African Sub 684 G=0.823 A=0.177
HapMap Asian Sub 250 G=0.748 A=0.252
HapMap Europe Sub 176 G=0.727 A=0.273
Korean Genome Project KOREAN Study-wide 1832 G=0.7566 A=0.2434
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.809 A=0.191
CNV burdens in cranial meningiomas Global Study-wide 790 G=0.724 A=0.276
CNV burdens in cranial meningiomas CRM Sub 790 G=0.724 A=0.276
Northern Sweden ACPOP Study-wide 600 G=0.827 A=0.173
Qatari Global Study-wide 216 G=0.708 A=0.292
SGDP_PRJ Global Study-wide 214 G=0.425 A=0.575
The Danish reference pan genome Danish Study-wide 40 G=0.80 A=0.20
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 38 G=0.63 A=0.37
Siberian Global Study-wide 22 G=0.50 A=0.50
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.47561431G>A
GRCh37.p13 chr 4 NC_000004.11:g.47563448G>A
Gene: ATP10D, ATPase phospholipid transporting 10D (putative) (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ATP10D transcript NM_020453.4:c.2668+356G>A 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
GRCh38.p14 chr 4 NC_000004.12:g.47561431= NC_000004.12:g.47561431G>A
GRCh37.p13 chr 4 NC_000004.11:g.47563448= NC_000004.11:g.47563448G>A
ATP10D transcript NM_020453.3:c.2668+356= NM_020453.3:c.2668+356G>A
ATP10D transcript NM_020453.4:c.2668+356= NM_020453.4:c.2668+356G>A
ATP10D transcript variant X1 XM_005248118.1:c.2668+356= XM_005248118.1:c.2668+356G>A
ATP10D transcript variant X2 XM_005248119.1:c.2623+356= XM_005248119.1:c.2623+356G>A
ATP10D transcript variant X3 XM_005248120.1:c.2668+356= XM_005248120.1:c.2668+356G>A
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#.

115 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 CSHL-HAPMAP ss19564817 Feb 27, 2004 (120)
2 CSHL-HAPMAP ss20194432 Feb 27, 2004 (120)
3 ABI ss42170217 Mar 14, 2006 (126)
4 ILLUMINA ss66826122 Nov 30, 2006 (127)
5 ILLUMINA ss66911509 Nov 30, 2006 (127)
6 ILLUMINA ss67044030 Nov 30, 2006 (127)
7 ILLUMINA ss70385362 May 17, 2007 (127)
8 ILLUMINA ss70509121 May 23, 2008 (130)
9 ILLUMINA ss71036211 May 17, 2007 (127)
10 ILLUMINA ss75916129 Dec 07, 2007 (129)
11 KRIBB_YJKIM ss85036108 Dec 14, 2007 (130)
12 BCMHGSC_JDW ss92561133 Mar 24, 2008 (129)
13 1000GENOMES ss112204353 Jan 25, 2009 (130)
14 ILLUMINA ss121421455 Dec 01, 2009 (131)
15 ENSEMBL ss139582554 Dec 01, 2009 (131)
16 ILLUMINA ss152882510 Dec 01, 2009 (131)
17 GMI ss157195276 Dec 01, 2009 (131)
18 ILLUMINA ss159154388 Dec 01, 2009 (131)
19 ENSEMBL ss161553752 Dec 01, 2009 (131)
20 COMPLETE_GENOMICS ss163415679 Jul 04, 2010 (132)
21 ILLUMINA ss169723121 Jul 04, 2010 (132)
22 ILLUMINA ss170781942 Jul 04, 2010 (132)
23 BCM-HGSC-SUB ss206575529 Jul 04, 2010 (132)
24 1000GENOMES ss220902872 Jul 14, 2010 (132)
25 1000GENOMES ss232375850 Jul 14, 2010 (132)
26 1000GENOMES ss239672432 Jul 15, 2010 (132)
27 GMI ss277686834 May 04, 2012 (137)
28 EXOME_CHIP ss491355432 May 04, 2012 (137)
29 ILLUMINA ss536655864 Sep 08, 2015 (146)
30 TISHKOFF ss557489029 Apr 25, 2013 (138)
31 SSMP ss651274434 Apr 25, 2013 (138)
32 ILLUMINA ss780680830 Sep 08, 2015 (146)
33 ILLUMINA ss783354121 Sep 08, 2015 (146)
34 ILLUMINA ss825354852 Apr 01, 2015 (144)
35 ILLUMINA ss832666999 Jul 13, 2019 (153)
36 EVA-GONL ss980064806 Aug 21, 2014 (142)
37 1000GENOMES ss1309539306 Aug 21, 2014 (142)
38 DDI ss1429864908 Apr 01, 2015 (144)
39 EVA_GENOME_DK ss1580536588 Apr 01, 2015 (144)
40 EVA_DECODE ss1589562580 Apr 01, 2015 (144)
41 EVA_UK10K_ALSPAC ss1609993794 Apr 01, 2015 (144)
42 EVA_UK10K_TWINSUK ss1652987827 Apr 01, 2015 (144)
43 EVA_SVP ss1712670246 Apr 01, 2015 (144)
44 ILLUMINA ss1752523925 Sep 08, 2015 (146)
45 HAMMER_LAB ss1801388906 Sep 08, 2015 (146)
46 ILLUMINA ss1917780208 Feb 12, 2016 (147)
47 WEILL_CORNELL_DGM ss1923296401 Feb 12, 2016 (147)
48 ILLUMINA ss1946115329 Feb 12, 2016 (147)
49 ILLUMINA ss1958679843 Feb 12, 2016 (147)
50 GENOMED ss1969728999 Jul 19, 2016 (147)
51 JJLAB ss2022234598 Sep 14, 2016 (149)
52 USC_VALOUEV ss2150345772 Dec 20, 2016 (150)
53 HUMAN_LONGEVITY ss2262685013 Dec 20, 2016 (150)
54 SYSTEMSBIOZJU ss2625617653 Nov 08, 2017 (151)
55 ILLUMINA ss2634115143 Nov 08, 2017 (151)
56 ILLUMINA ss2634115144 Nov 08, 2017 (151)
57 GRF ss2705802174 Nov 08, 2017 (151)
58 ILLUMINA ss2711004474 Nov 08, 2017 (151)
59 GNOMAD ss2808715879 Nov 08, 2017 (151)
60 AFFY ss2985291529 Nov 08, 2017 (151)
61 AFFY ss2985914836 Nov 08, 2017 (151)
62 SWEGEN ss2994585554 Nov 08, 2017 (151)
63 ILLUMINA ss3022369652 Nov 08, 2017 (151)
64 BIOINF_KMB_FNS_UNIBA ss3024887590 Nov 08, 2017 (151)
65 CSHL ss3345680541 Nov 08, 2017 (151)
66 ILLUMINA ss3628957598 Oct 12, 2018 (152)
67 ILLUMINA ss3628957599 Oct 12, 2018 (152)
68 ILLUMINA ss3634950817 Oct 12, 2018 (152)
69 ILLUMINA ss3638484687 Oct 12, 2018 (152)
70 ILLUMINA ss3639245434 Oct 12, 2018 (152)
71 ILLUMINA ss3639643610 Oct 12, 2018 (152)
72 ILLUMINA ss3640658113 Oct 12, 2018 (152)
73 ILLUMINA ss3643436173 Oct 12, 2018 (152)
74 ILLUMINA ss3644848100 Oct 12, 2018 (152)
75 ILLUMINA ss3652854065 Oct 12, 2018 (152)
76 ILLUMINA ss3654062388 Oct 12, 2018 (152)
77 EGCUT_WGS ss3662511214 Jul 13, 2019 (153)
78 EVA_DECODE ss3711957357 Jul 13, 2019 (153)
79 ILLUMINA ss3726129826 Jul 13, 2019 (153)
80 ACPOP ss3731107122 Jul 13, 2019 (153)
81 ILLUMINA ss3744524571 Jul 13, 2019 (153)
82 ILLUMINA ss3745251073 Jul 13, 2019 (153)
83 EVA ss3761743189 Jul 13, 2019 (153)
84 PAGE_CC ss3771121644 Jul 13, 2019 (153)
85 ILLUMINA ss3772745744 Jul 13, 2019 (153)
86 PACBIO ss3784697217 Jul 13, 2019 (153)
87 PACBIO ss3790157454 Jul 13, 2019 (153)
88 PACBIO ss3795032695 Jul 13, 2019 (153)
89 KHV_HUMAN_GENOMES ss3804876817 Jul 13, 2019 (153)
90 EVA ss3828515608 Apr 26, 2020 (154)
91 HGDP ss3847749454 Apr 26, 2020 (154)
92 SGDP_PRJ ss3858808961 Apr 26, 2020 (154)
93 KRGDB ss3904997062 Apr 26, 2020 (154)
94 KOGIC ss3954035155 Apr 26, 2020 (154)
95 EVA ss3984527573 Apr 26, 2021 (155)
96 EVA ss3985067846 Apr 26, 2021 (155)
97 EVA ss4017144369 Apr 26, 2021 (155)
98 TOPMED ss4612227741 Apr 26, 2021 (155)
99 TOMMO_GENOMICS ss5165425736 Apr 26, 2021 (155)
100 EVA ss5237348513 Apr 26, 2021 (155)
101 1000G_HIGH_COVERAGE ss5259014213 Oct 13, 2022 (156)
102 EVA ss5314955664 Oct 13, 2022 (156)
103 HUGCELL_USP ss5457818662 Oct 13, 2022 (156)
104 EVA ss5507496110 Oct 13, 2022 (156)
105 1000G_HIGH_COVERAGE ss5539965730 Oct 13, 2022 (156)
106 SANFORD_IMAGENETICS ss5624554727 Oct 13, 2022 (156)
107 SANFORD_IMAGENETICS ss5634913825 Oct 13, 2022 (156)
108 TOMMO_GENOMICS ss5699413020 Oct 13, 2022 (156)
109 YY_MCH ss5805006926 Oct 13, 2022 (156)
110 EVA ss5843926835 Oct 13, 2022 (156)
111 EVA ss5847242502 Oct 13, 2022 (156)
112 EVA ss5854202973 Oct 13, 2022 (156)
113 EVA ss5863260377 Oct 13, 2022 (156)
114 EVA ss5963310874 Oct 13, 2022 (156)
115 EVA ss5979699026 Oct 13, 2022 (156)
116 1000Genomes NC_000004.11 - 47563448 Oct 12, 2018 (152)
117 1000Genomes_30x NC_000004.12 - 47561431 Oct 13, 2022 (156)
118 The Avon Longitudinal Study of Parents and Children NC_000004.11 - 47563448 Oct 12, 2018 (152)
119 Genetic variation in the Estonian population NC_000004.11 - 47563448 Oct 12, 2018 (152)
120 The Danish reference pan genome NC_000004.11 - 47563448 Apr 26, 2020 (154)
121 gnomAD - Genomes NC_000004.12 - 47561431 Apr 26, 2021 (155)
122 Genome of the Netherlands Release 5 NC_000004.11 - 47563448 Apr 26, 2020 (154)
123 HGDP-CEPH-db Supplement 1 NC_000004.10 - 47258205 Apr 26, 2020 (154)
124 HapMap NC_000004.12 - 47561431 Apr 26, 2020 (154)
125 KOREAN population from KRGDB NC_000004.11 - 47563448 Apr 26, 2020 (154)
126 Korean Genome Project NC_000004.12 - 47561431 Apr 26, 2020 (154)
127 Northern Sweden NC_000004.11 - 47563448 Jul 13, 2019 (153)
128 The PAGE Study NC_000004.12 - 47561431 Jul 13, 2019 (153)
129 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000004.11 - 47563448 Apr 26, 2021 (155)
130 CNV burdens in cranial meningiomas NC_000004.11 - 47563448 Apr 26, 2021 (155)
131 Qatari NC_000004.11 - 47563448 Apr 26, 2020 (154)
132 SGDP_PRJ NC_000004.11 - 47563448 Apr 26, 2020 (154)
133 Siberian NC_000004.11 - 47563448 Apr 26, 2020 (154)
134 8.3KJPN NC_000004.11 - 47563448 Apr 26, 2021 (155)
135 14KJPN NC_000004.12 - 47561431 Oct 13, 2022 (156)
136 TopMed NC_000004.12 - 47561431 Apr 26, 2021 (155)
137 UK 10K study - Twins NC_000004.11 - 47563448 Oct 12, 2018 (152)
138 ALFA NC_000004.12 - 47561431 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)
rs57083896 May 23, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss3639245434, ss3639643610 NC_000004.9:47404375:G:A NC_000004.12:47561430:G:A (self)
427346, ss92561133, ss112204353, ss163415679, ss206575529, ss277686834, ss825354852, ss1589562580, ss1712670246, ss3643436173, ss3847749454 NC_000004.10:47258204:G:A NC_000004.12:47561430:G:A (self)
20928192, 11657683, 8249462, 6701527, 5138634, 12174456, 4391987, 293773, 76933, 5338331, 10825941, 2862126, 23395043, 11657683, ss220902872, ss232375850, ss239672432, ss491355432, ss536655864, ss557489029, ss651274434, ss780680830, ss783354121, ss832666999, ss980064806, ss1309539306, ss1429864908, ss1580536588, ss1609993794, ss1652987827, ss1752523925, ss1801388906, ss1917780208, ss1923296401, ss1946115329, ss1958679843, ss1969728999, ss2022234598, ss2150345772, ss2625617653, ss2634115143, ss2634115144, ss2705802174, ss2711004474, ss2808715879, ss2985291529, ss2985914836, ss2994585554, ss3022369652, ss3345680541, ss3628957598, ss3628957599, ss3634950817, ss3638484687, ss3640658113, ss3644848100, ss3652854065, ss3654062388, ss3662511214, ss3731107122, ss3744524571, ss3745251073, ss3761743189, ss3772745744, ss3784697217, ss3790157454, ss3795032695, ss3828515608, ss3858808961, ss3904997062, ss3984527573, ss3985067846, ss4017144369, ss5165425736, ss5237348513, ss5314955664, ss5507496110, ss5624554727, ss5634913825, ss5843926835, ss5847242502, ss5963310874, ss5979699026 NC_000004.11:47563447:G:A NC_000004.12:47561430:G:A (self)
27491665, 148161549, 2607791, 10413156, 343113, 33250124, 449605297, 13326889071, ss2262685013, ss3024887590, ss3711957357, ss3726129826, ss3771121644, ss3804876817, ss3954035155, ss4612227741, ss5259014213, ss5457818662, ss5539965730, ss5699413020, ss5805006926, ss5854202973, ss5863260377 NC_000004.12:47561430:G:A NC_000004.12:47561430:G:A (self)
ss19564817, ss20194432 NT_006238.10:7265413:G:A NC_000004.12:47561430:G:A (self)
ss42170217, ss66826122, ss66911509, ss67044030, ss70385362, ss70509121, ss71036211, ss75916129, ss85036108, ss121421455, ss139582554, ss152882510, ss157195276, ss159154388, ss161553752, ss169723121, ss170781942 NT_006238.11:7266351:G:A NC_000004.12:47561430: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.

1 citation for rs10938494
PMID Title Author Year Journal
19798445 Genetic determinants of circulating sphingolipid concentrations in European populations. Hicks AA et al. 2009 PLoS 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