Skip to main page content
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.

rs131

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr7:24899268 (GRCh38.p13) 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
C>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.413937 (109565/264690, TOPMED)
G=0.403875 (56507/139912, GnomAD)
G=0.47314 (37235/78698, PAGE_STUDY) (+ 17 more)
G=0.39158 (7397/18890, ALFA)
C=0.24179 (4052/16758, 8.3KJPN)
C=0.4922 (2465/5008, 1000G)
G=0.3888 (1742/4480, Estonian)
G=0.3747 (1444/3854, ALSPAC)
G=0.3865 (1433/3708, TWINSUK)
C=0.2693 (789/2930, KOREAN)
G=0.3675 (416/1132, Daghestan)
G=0.358 (357/998, GoNL)
G=0.408 (245/600, NorthernSweden)
C=0.331 (129/390, SGDP_PRJ)
C=0.494 (162/328, HapMap)
G=0.292 (63/216, Qatari)
C=0.297 (63/212, Vietnamese)
G=0.327 (34/104, Ancient Sardinia)
C=0.36 (16/44, Siberian)
G=0.38 (15/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
OSBPL3 : Intron 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.p13 chr 7 NC_000007.14:g.24899268C>G
GRCh37.p13 chr 7 NC_000007.13:g.24938887C>G
Gene: OSBPL3, oxysterol binding protein like 3 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
OSBPL3 transcript variant 1 NM_015550.4:c.-149-6647G>C N/A Intron Variant
OSBPL3 transcript variant 2 NM_145320.2:c. N/A Genic Upstream Transcript Variant
OSBPL3 transcript variant 3 NM_145321.2:c. N/A Genic Upstream Transcript Variant
OSBPL3 transcript variant 4 NM_145322.2:c. N/A Genic Upstream Transcript Variant
OSBPL3 transcript variant 5 NR_104111.1:n. N/A Genic Upstream Transcript Variant
OSBPL3 transcript variant 6 NR_104112.1:n. N/A Genic Upstream Transcript Variant
OSBPL3 transcript variant X2 XM_005249698.3:c.-149-664…

XM_005249698.3:c.-149-6647G>C

N/A Intron Variant
OSBPL3 transcript variant X3 XM_006715681.3:c.-149-664…

XM_006715681.3:c.-149-6647G>C

N/A Intron Variant
OSBPL3 transcript variant X4 XM_006715682.3:c.-149-664…

XM_006715682.3:c.-149-6647G>C

N/A Intron Variant
OSBPL3 transcript variant X7 XM_006715683.3:c.-149-664…

XM_006715683.3:c.-149-6647G>C

N/A Intron Variant
OSBPL3 transcript variant X15 XM_006715684.4:c.-1192-66…

XM_006715684.4:c.-1192-6647G>C

N/A Intron Variant
OSBPL3 transcript variant X1 XM_011515258.2:c.-149-664…

XM_011515258.2:c.-149-6647G>C

N/A Intron Variant
OSBPL3 transcript variant X5 XM_011515259.2:c.-628-664…

XM_011515259.2:c.-628-6647G>C

N/A Intron Variant
OSBPL3 transcript variant X6 XM_017011948.1:c.-491-664…

XM_017011948.1:c.-491-6647G>C

N/A Intron Variant
OSBPL3 transcript variant X8 XM_017011949.1:c.-628-664…

XM_017011949.1:c.-628-6647G>C

N/A Intron Variant
OSBPL3 transcript variant X13 XR_001744620.1:n. N/A Intron Variant
OSBPL3 transcript variant X9 XR_428073.3:n. N/A Intron Variant
OSBPL3 transcript variant X11 XR_428074.3:n. N/A Intron Variant
OSBPL3 transcript variant X12 XR_428075.3:n. N/A Intron Variant
OSBPL3 transcript variant X10 XR_926927.2:n. N/A Intron Variant
OSBPL3 transcript variant X14 XR_926929.1:n. 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

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 18890 C=0.60842 G=0.39158
European Sub 14286 C=0.62642 G=0.37358
African Sub 2946 C=0.5611 G=0.4389
African Others Sub 114 C=0.509 G=0.491
African American Sub 2832 C=0.5632 G=0.4368
Asian Sub 112 C=0.295 G=0.705
East Asian Sub 86 C=0.28 G=0.72
Other Asian Sub 26 C=0.35 G=0.65
Latin American 1 Sub 146 C=0.664 G=0.336
Latin American 2 Sub 610 C=0.531 G=0.469
South Asian Sub 98 C=0.43 G=0.57
Other Sub 692 C=0.571 G=0.429


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 C=0.586063 G=0.413937
gnomAD - Genomes Global Study-wide 139912 C=0.596125 G=0.403875
gnomAD - Genomes European Sub 75794 C=0.63166 G=0.36834
gnomAD - Genomes African Sub 41884 C=0.56485 G=0.43515
gnomAD - Genomes American Sub 13642 C=0.56143 G=0.43857
gnomAD - Genomes Ashkenazi Jewish Sub 3322 C=0.5993 G=0.4007
gnomAD - Genomes East Asian Sub 3116 C=0.2959 G=0.7041
gnomAD - Genomes Other Sub 2154 C=0.6031 G=0.3969
The PAGE Study Global Study-wide 78698 C=0.52686 G=0.47314
The PAGE Study AfricanAmerican Sub 32516 C=0.56341 G=0.43659
The PAGE Study Mexican Sub 10810 C=0.55652 G=0.44348
The PAGE Study Asian Sub 8318 C=0.2372 G=0.7628
The PAGE Study PuertoRican Sub 7918 C=0.6286 G=0.3714
The PAGE Study NativeHawaiian Sub 4534 C=0.3617 G=0.6383
The PAGE Study Cuban Sub 4228 C=0.6313 G=0.3687
The PAGE Study Dominican Sub 3828 C=0.6118 G=0.3882
The PAGE Study CentralAmerican Sub 2450 C=0.5286 G=0.4714
The PAGE Study SouthAmerican Sub 1980 C=0.5434 G=0.4566
The PAGE Study NativeAmerican Sub 1260 C=0.6151 G=0.3849
The PAGE Study SouthAsian Sub 856 C=0.444 G=0.556
1000Genomes Global Study-wide 5008 C=0.4922 G=0.5078
1000Genomes African Sub 1322 C=0.5620 G=0.4380
1000Genomes East Asian Sub 1008 C=0.2738 G=0.7262
1000Genomes Europe Sub 1006 C=0.6362 G=0.3638
1000Genomes South Asian Sub 978 C=0.439 G=0.561
1000Genomes American Sub 694 C=0.543 G=0.457
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.6112 G=0.3888
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.6253 G=0.3747
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.6135 G=0.3865
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.2693 G=0.7307
Genome-wide autozygosity in Daghestan Global Study-wide 1132 C=0.6325 G=0.3675
Genome-wide autozygosity in Daghestan Daghestan Sub 626 C=0.703 G=0.297
Genome-wide autozygosity in Daghestan Near_East Sub 144 C=0.611 G=0.389
Genome-wide autozygosity in Daghestan Central Asia Sub 120 C=0.458 G=0.542
Genome-wide autozygosity in Daghestan Europe Sub 108 C=0.620 G=0.380
Genome-wide autozygosity in Daghestan South Asian Sub 98 C=0.43 G=0.57
Genome-wide autozygosity in Daghestan Caucasus Sub 36 C=0.67 G=0.33
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.642 G=0.358
Northern Sweden ACPOP Study-wide 600 C=0.592 G=0.408
SGDP_PRJ Global Study-wide 390 C=0.331 G=0.669
HapMap Global Study-wide 328 C=0.494 G=0.506
HapMap African Sub 120 C=0.575 G=0.425
HapMap American Sub 120 C=0.658 G=0.342
HapMap Asian Sub 88 C=0.16 G=0.84
Qatari Global Study-wide 216 C=0.708 G=0.292
A Vietnamese Genetic Variation Database Global Study-wide 212 C=0.297 G=0.703
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 104 C=0.673 G=0.327
Siberian Global Study-wide 44 C=0.36 G=0.64
The Danish reference pan genome Danish Study-wide 40 C=0.62 G=0.38
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 C= G
GRCh38.p13 chr 7 NC_000007.14:g.24899268= NC_000007.14:g.24899268C>G
GRCh37.p13 chr 7 NC_000007.13:g.24938887= NC_000007.13:g.24938887C>G
OSBPL3 transcript variant 1 NM_015550.2:c.-149-6647= NM_015550.2:c.-149-6647G>C
OSBPL3 transcript variant 1 NM_015550.4:c.-149-6647= NM_015550.4:c.-149-6647G>C
OSBPL3 transcript variant 2 NM_145320.1:c.-149-6647= NM_145320.1:c.-149-6647G>C
OSBPL3 transcript variant 3 NM_145321.1:c.-149-6647= NM_145321.1:c.-149-6647G>C
OSBPL3 transcript variant 4 NM_145322.1:c.-149-6647= NM_145322.1:c.-149-6647G>C
OSBPL3 transcript variant X1 XM_005249698.1:c.-149-6647= XM_005249698.1:c.-149-6647G>C
OSBPL3 transcript variant X2 XM_005249698.3:c.-149-6647= XM_005249698.3:c.-149-6647G>C
OSBPL3 transcript variant X3 XM_006715681.3:c.-149-6647= XM_006715681.3:c.-149-6647G>C
OSBPL3 transcript variant X4 XM_006715682.3:c.-149-6647= XM_006715682.3:c.-149-6647G>C
OSBPL3 transcript variant X7 XM_006715683.3:c.-149-6647= XM_006715683.3:c.-149-6647G>C
OSBPL3 transcript variant X15 XM_006715684.4:c.-1192-6647= XM_006715684.4:c.-1192-6647G>C
OSBPL3 transcript variant X1 XM_011515258.2:c.-149-6647= XM_011515258.2:c.-149-6647G>C
OSBPL3 transcript variant X5 XM_011515259.2:c.-628-6647= XM_011515259.2:c.-628-6647G>C
OSBPL3 transcript variant X6 XM_017011948.1:c.-491-6647= XM_017011948.1:c.-491-6647G>C
OSBPL3 transcript variant X8 XM_017011949.1:c.-628-6647= XM_017011949.1:c.-628-6647G>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#.

83 SubSNP, 20 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss131 Sep 19, 2000 (36)
2 TSC-CSHL ss1494696 Oct 04, 2000 (86)
3 SC_JCM ss6080518 Feb 20, 2003 (111)
4 BCM_SSAHASNP ss10380474 Jul 11, 2003 (116)
5 WI_SSAHASNP ss11871427 Jul 11, 2003 (116)
6 WUGSC_SSAHASNP ss14561184 Dec 05, 2003 (120)
7 CSHL-HAPMAP ss17169805 Feb 27, 2004 (120)
8 SSAHASNP ss22632237 Apr 05, 2004 (121)
9 PERLEGEN ss23404583 Sep 20, 2004 (123)
10 ABI ss44829259 Mar 14, 2006 (126)
11 AFFY ss65968919 Nov 30, 2006 (127)
12 PERLEGEN ss69009662 May 17, 2007 (127)
13 HGSV ss78828062 Dec 06, 2007 (129)
14 BCMHGSC_JDW ss93646230 Mar 24, 2008 (129)
15 HUMANGENOME_JCVI ss98240999 Feb 04, 2009 (130)
16 1000GENOMES ss111690908 Jan 25, 2009 (130)
17 ILLUMINA-UK ss115987541 Feb 14, 2009 (130)
18 ENSEMBL ss142760218 Dec 01, 2009 (131)
19 ENSEMBL ss143685043 Dec 01, 2009 (131)
20 GMI ss154528743 Dec 01, 2009 (131)
21 COMPLETE_GENOMICS ss166294570 Jul 04, 2010 (132)
22 BUSHMAN ss203089132 Jul 04, 2010 (132)
23 1000GENOMES ss212009541 Jul 14, 2010 (132)
24 1000GENOMES ss222968521 Jul 14, 2010 (132)
25 1000GENOMES ss233894339 Jul 15, 2010 (132)
26 1000GENOMES ss240865896 Jul 15, 2010 (132)
27 BL ss254127922 May 09, 2011 (134)
28 GMI ss279229017 May 04, 2012 (137)
29 PJP ss294032219 May 09, 2011 (134)
30 ILLUMINA ss479771021 May 04, 2012 (137)
31 ILLUMINA ss485409135 May 04, 2012 (137)
32 ILLUMINA ss533266309 Sep 08, 2015 (146)
33 TISHKOFF ss559875586 Apr 25, 2013 (138)
34 SSMP ss654228889 Apr 25, 2013 (138)
35 ILLUMINA ss779648723 Aug 21, 2014 (142)
36 ILLUMINA ss781064438 Aug 21, 2014 (142)
37 ILLUMINA ss835121714 Aug 21, 2014 (142)
38 EVA-GONL ss984063895 Aug 21, 2014 (142)
39 JMKIDD_LAB ss1074451246 Aug 21, 2014 (142)
40 1000GENOMES ss1324345457 Aug 21, 2014 (142)
41 HAMMER_LAB ss1397488209 Sep 08, 2015 (146)
42 DDI ss1431061145 Apr 01, 2015 (144)
43 EVA_GENOME_DK ss1582116568 Apr 01, 2015 (144)
44 EVA_DECODE ss1593632744 Apr 01, 2015 (144)
45 EVA_UK10K_ALSPAC ss1617793828 Apr 01, 2015 (144)
46 EVA_UK10K_TWINSUK ss1660787861 Apr 01, 2015 (144)
47 HAMMER_LAB ss1804916722 Sep 08, 2015 (146)
48 WEILL_CORNELL_DGM ss1927308949 Feb 12, 2016 (147)
49 ILLUMINA ss1958996467 Feb 12, 2016 (147)
50 GENOMED ss1970651530 Jul 19, 2016 (147)
51 JJLAB ss2024331537 Sep 14, 2016 (149)
52 USC_VALOUEV ss2152527682 Dec 20, 2016 (150)
53 HUMAN_LONGEVITY ss2292524763 Dec 20, 2016 (150)
54 TOPMED ss2461385534 Dec 20, 2016 (150)
55 SYSTEMSBIOZJU ss2626654714 Nov 08, 2017 (151)
56 ILLUMINA ss2634581248 Nov 08, 2017 (151)
57 GRF ss2708184506 Nov 08, 2017 (151)
58 GNOMAD ss2850927534 Nov 08, 2017 (151)
59 SWEGEN ss3000793893 Nov 08, 2017 (151)
60 ILLUMINA ss3022718071 Nov 08, 2017 (151)
61 BIOINF_KMB_FNS_UNIBA ss3025960069 Nov 08, 2017 (151)
62 CSHL ss3347488194 Nov 08, 2017 (151)
63 TOPMED ss3525169808 Nov 08, 2017 (151)
64 ILLUMINA ss3629774430 Oct 12, 2018 (152)
65 ILLUMINA ss3632490027 Oct 12, 2018 (152)
66 ILLUMINA ss3642551651 Oct 12, 2018 (152)
67 URBANLAB ss3648585740 Oct 12, 2018 (152)
68 ILLUMINA ss3653246293 Oct 12, 2018 (152)
69 EGCUT_WGS ss3668722657 Jul 13, 2019 (153)
70 EVA_DECODE ss3719304062 Jul 13, 2019 (153)
71 ILLUMINA ss3726429326 Jul 13, 2019 (153)
72 ACPOP ss3734451681 Jul 13, 2019 (153)
73 EVA ss3766316576 Jul 13, 2019 (153)
74 PAGE_CC ss3771358346 Jul 13, 2019 (153)
75 KHV_HUMAN_GENOMES ss3809483992 Jul 13, 2019 (153)
76 EVA ss3830470461 Apr 26, 2020 (154)
77 EVA ss3838722480 Apr 26, 2020 (154)
78 EVA ss3844173734 Apr 26, 2020 (154)
79 SGDP_PRJ ss3866852846 Apr 26, 2020 (154)
80 KRGDB ss3913891144 Apr 26, 2020 (154)
81 EVA ss3985283822 Apr 26, 2021 (155)
82 TOPMED ss4739173897 Apr 26, 2021 (155)
83 TOMMO_GENOMICS ss5182268780 Apr 26, 2021 (155)
84 1000Genomes NC_000007.13 - 24938887 Oct 12, 2018 (152)
85 The Avon Longitudinal Study of Parents and Children NC_000007.13 - 24938887 Oct 12, 2018 (152)
86 Genome-wide autozygosity in Daghestan NC_000007.12 - 24905412 Apr 26, 2020 (154)
87 Genetic variation in the Estonian population NC_000007.13 - 24938887 Oct 12, 2018 (152)
88 The Danish reference pan genome NC_000007.13 - 24938887 Apr 26, 2020 (154)
89 gnomAD - Genomes NC_000007.14 - 24899268 Apr 26, 2021 (155)
90 Genome of the Netherlands Release 5 NC_000007.13 - 24938887 Apr 26, 2020 (154)
91 HapMap NC_000007.14 - 24899268 Apr 26, 2020 (154)
92 KOREAN population from KRGDB NC_000007.13 - 24938887 Apr 26, 2020 (154)
93 Northern Sweden NC_000007.13 - 24938887 Jul 13, 2019 (153)
94 The PAGE Study NC_000007.14 - 24899268 Jul 13, 2019 (153)
95 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000007.13 - 24938887 Apr 26, 2021 (155)
96 Qatari NC_000007.13 - 24938887 Apr 26, 2020 (154)
97 SGDP_PRJ NC_000007.13 - 24938887 Apr 26, 2020 (154)
98 Siberian NC_000007.13 - 24938887 Apr 26, 2020 (154)
99 8.3KJPN NC_000007.13 - 24938887 Apr 26, 2021 (155)
100 TopMed NC_000007.14 - 24899268 Apr 26, 2021 (155)
101 UK 10K study - Twins NC_000007.13 - 24938887 Oct 12, 2018 (152)
102 A Vietnamese Genetic Variation Database NC_000007.13 - 24938887 Jul 13, 2019 (153)
103 ALFA NC_000007.14 - 24899268 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)
rs10355835 Feb 27, 2004 (120)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss78828062 NC_000007.11:24712126:C:G NC_000007.14:24899267:C:G (self)
462463, ss93646230, ss111690908, ss115987541, ss166294570, ss203089132, ss212009541, ss254127922, ss279229017, ss294032219, ss485409135, ss1397488209, ss1593632744 NC_000007.12:24905411:C:G NC_000007.14:24899267:C:G (self)
36287396, 20229699, 14460905, 8281507, 9019542, 21068538, 7736546, 509749, 9350879, 18869826, 5044036, 40238087, 20229699, 4507484, ss222968521, ss233894339, ss240865896, ss479771021, ss533266309, ss559875586, ss654228889, ss779648723, ss781064438, ss835121714, ss984063895, ss1074451246, ss1324345457, ss1431061145, ss1582116568, ss1617793828, ss1660787861, ss1804916722, ss1927308949, ss1958996467, ss1970651530, ss2024331537, ss2152527682, ss2461385534, ss2626654714, ss2634581248, ss2708184506, ss2850927534, ss3000793893, ss3022718071, ss3347488194, ss3629774430, ss3632490027, ss3642551651, ss3653246293, ss3668722657, ss3734451681, ss3766316576, ss3830470461, ss3838722480, ss3866852846, ss3913891144, ss3985283822, ss5182268780 NC_000007.13:24938886:C:G NC_000007.14:24899267:C:G (self)
255867379, 3358794, 579815, 360667086, 576551456, 3159725142, ss2292524763, ss3025960069, ss3525169808, ss3648585740, ss3719304062, ss3726429326, ss3771358346, ss3809483992, ss3844173734, ss4739173897 NC_000007.14:24899267:C:G NC_000007.14:24899267:C:G (self)
ss10380474, ss11871427 NT_007819.13:24232494:C:G NC_000007.14:24899267:C:G (self)
ss14561184, ss17169805, ss22632237 NT_007819.14:24232494:C:G NC_000007.14:24899267:C:G (self)
ss131, ss1494696, ss6080518, ss23404583, ss44829259, ss65968919, ss69009662, ss98240999, ss142760218, ss143685043, ss154528743 NT_007819.17:24928886:C:G NC_000007.14:24899267:C:G (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 rs131

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.post596+ae089ad