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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.

rs158

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr7:24978343 (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 / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.138895 (36764/264690, TOPMED)
C=0.148984 (20892/140230, GnomAD)
C=0.17440 (6094/34942, ALFA) (+ 16 more)
C=0.22980 (3851/16758, 8.3KJPN)
C=0.1214 (608/5008, 1000G)
C=0.1808 (810/4480, Estonian)
C=0.2177 (839/3854, ALSPAC)
C=0.2025 (751/3708, TWINSUK)
C=0.1765 (517/2930, KOREAN)
C=0.1075 (203/1888, HapMap)
C=0.1807 (331/1832, Korea1K)
C=0.222 (222/998, GoNL)
C=0.213 (128/600, NorthernSweden)
C=0.095 (52/546, SGDP_PRJ)
C=0.097 (21/216, Qatari)
C=0.125 (27/216, Vietnamese)
C=0.13 (7/54, Siberian)
C=0.35 (14/40, GENOME_DK)
C=0.29 (10/34, Ancient Sardinia)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
OSBPL3 : Intron Variant
Publications
1 citation
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.24978343C>G
GRCh38.p13 chr 7 NC_000007.14:g.24978343C>T
GRCh37.p13 chr 7 NC_000007.13:g.25017962C>G
GRCh37.p13 chr 7 NC_000007.13:g.25017962C>T
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.-150+1543G>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 X3 XM_006715681.3:c.-150+154…

XM_006715681.3:c.-150+1543G>C

N/A Intron Variant
OSBPL3 transcript variant X4 XM_006715682.3:c.-150+154…

XM_006715682.3:c.-150+1543G>C

N/A Intron Variant
OSBPL3 transcript variant X7 XM_006715683.3:c.-150+154…

XM_006715683.3:c.-150+1543G>C

N/A Intron Variant
OSBPL3 transcript variant X15 XM_006715684.4:c.-1193+15…

XM_006715684.4:c.-1193+1543G>C

N/A Intron Variant
OSBPL3 transcript variant X5 XM_011515259.2:c.-629+154…

XM_011515259.2:c.-629+1543G>C

N/A Intron Variant
OSBPL3 transcript variant X6 XM_017011948.1:c.-492+154…

XM_017011948.1:c.-492+1543G>C

N/A Intron Variant
OSBPL3 transcript variant X8 XM_017011949.1:c.-629+154…

XM_017011949.1:c.-629+1543G>C

N/A Intron Variant
OSBPL3 transcript variant X2 XM_005249698.3:c. N/A Genic Upstream Transcript Variant
OSBPL3 transcript variant X1 XM_011515258.2:c. N/A Genic Upstream Transcript 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 34942 C=0.17440 T=0.82560
European Sub 26104 C=0.19863 T=0.80137
African Sub 3838 C=0.0500 T=0.9500
African Others Sub 136 C=0.037 T=0.963
African American Sub 3702 C=0.0505 T=0.9495
Asian Sub 176 C=0.114 T=0.886
East Asian Sub 116 C=0.164 T=0.836
Other Asian Sub 60 C=0.02 T=0.98
Latin American 1 Sub 274 C=0.106 T=0.894
Latin American 2 Sub 1996 C=0.1318 T=0.8682
South Asian Sub 126 C=0.095 T=0.905
Other Sub 2428 C=0.1619 T=0.8381


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=0.138895 T=0.861105
gnomAD - Genomes Global Study-wide 140230 C=0.148984 T=0.851016
gnomAD - Genomes European Sub 75904 C=0.20435 T=0.79565
gnomAD - Genomes African Sub 42056 C=0.05157 T=0.94843
gnomAD - Genomes American Sub 13660 C=0.12767 T=0.87233
gnomAD - Genomes Ashkenazi Jewish Sub 3324 C=0.2025 T=0.7975
gnomAD - Genomes East Asian Sub 3134 C=0.1551 T=0.8449
gnomAD - Genomes Other Sub 2152 C=0.1436 T=0.8564
8.3KJPN JAPANESE Study-wide 16758 C=0.22980 T=0.77020
1000Genomes Global Study-wide 5008 C=0.1214 T=0.8786
1000Genomes African Sub 1322 C=0.0310 T=0.9690
1000Genomes East Asian Sub 1008 C=0.1766 T=0.8234
1000Genomes Europe Sub 1006 C=0.2187 T=0.7813
1000Genomes South Asian Sub 978 C=0.076 T=0.924
1000Genomes American Sub 694 C=0.137 T=0.863
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.1808 T=0.8192
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.2177 T=0.7823
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.2025 T=0.7975
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.1765 G=0.0000, T=0.8235
HapMap Global Study-wide 1888 C=0.1075 T=0.8925
HapMap American Sub 768 C=0.121 T=0.879
HapMap African Sub 690 C=0.035 T=0.965
HapMap Asian Sub 254 C=0.201 T=0.799
HapMap Europe Sub 176 C=0.199 T=0.801
Korean Genome Project KOREAN Study-wide 1832 C=0.1807 T=0.8193
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.222 T=0.778
Northern Sweden ACPOP Study-wide 600 C=0.213 T=0.787
SGDP_PRJ Global Study-wide 546 C=0.095 T=0.905
Qatari Global Study-wide 216 C=0.097 T=0.903
A Vietnamese Genetic Variation Database Global Study-wide 216 C=0.125 T=0.875
Siberian Global Study-wide 54 C=0.13 T=0.87
The Danish reference pan genome Danish Study-wide 40 C=0.35 T=0.65
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 34 C=0.29 T=0.71
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 T
GRCh38.p13 chr 7 NC_000007.14:g.24978343= NC_000007.14:g.24978343C>G NC_000007.14:g.24978343C>T
GRCh37.p13 chr 7 NC_000007.13:g.25017962= NC_000007.13:g.25017962C>G NC_000007.13:g.25017962C>T
OSBPL3 transcript variant 1 NM_015550.2:c.-150+1543= NM_015550.2:c.-150+1543G>C NM_015550.2:c.-150+1543G>A
OSBPL3 transcript variant 1 NM_015550.4:c.-150+1543= NM_015550.4:c.-150+1543G>C NM_015550.4:c.-150+1543G>A
OSBPL3 transcript variant 2 NM_145320.1:c.-150+1543= NM_145320.1:c.-150+1543G>C NM_145320.1:c.-150+1543G>A
OSBPL3 transcript variant 3 NM_145321.1:c.-150+1543= NM_145321.1:c.-150+1543G>C NM_145321.1:c.-150+1543G>A
OSBPL3 transcript variant 4 NM_145322.1:c.-150+1543= NM_145322.1:c.-150+1543G>C NM_145322.1:c.-150+1543G>A
OSBPL3 transcript variant X3 XM_006715681.3:c.-150+1543= XM_006715681.3:c.-150+1543G>C XM_006715681.3:c.-150+1543G>A
OSBPL3 transcript variant X4 XM_006715682.3:c.-150+1543= XM_006715682.3:c.-150+1543G>C XM_006715682.3:c.-150+1543G>A
OSBPL3 transcript variant X7 XM_006715683.3:c.-150+1543= XM_006715683.3:c.-150+1543G>C XM_006715683.3:c.-150+1543G>A
OSBPL3 transcript variant X15 XM_006715684.4:c.-1193+1543= XM_006715684.4:c.-1193+1543G>C XM_006715684.4:c.-1193+1543G>A
OSBPL3 transcript variant X5 XM_011515259.2:c.-629+1543= XM_011515259.2:c.-629+1543G>C XM_011515259.2:c.-629+1543G>A
OSBPL3 transcript variant X6 XM_017011948.1:c.-492+1543= XM_017011948.1:c.-492+1543G>C XM_017011948.1:c.-492+1543G>A
OSBPL3 transcript variant X8 XM_017011949.1:c.-629+1543= XM_017011949.1:c.-629+1543G>C XM_017011949.1:c.-629+1543G>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#.

92 SubSNP, 19 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss158 Sep 19, 2000 (36)
2 SC_JCM ss3830883 Sep 28, 2001 (100)
3 WI_SSAHASNP ss6504381 Feb 20, 2003 (111)
4 BCM_SSAHASNP ss10414866 Jul 11, 2003 (116)
5 WUGSC_SSAHASNP ss14574621 Dec 05, 2003 (120)
6 BCM_SSAHASNP ss14734392 Dec 05, 2003 (120)
7 CSHL-HAPMAP ss17941371 Feb 27, 2004 (120)
8 CSHL-HAPMAP ss19722158 Feb 27, 2004 (120)
9 CSHL-HAPMAP ss20317745 Feb 27, 2004 (120)
10 SSAHASNP ss22562848 Apr 05, 2004 (121)
11 SSAHASNP ss22943051 Apr 05, 2004 (121)
12 AFFY ss76593613 Dec 07, 2007 (129)
13 HGSV ss78206681 Dec 07, 2007 (129)
14 HGSV ss81345663 Dec 15, 2007 (130)
15 HGSV ss82638472 Dec 15, 2007 (130)
16 HGSV ss84903580 Dec 15, 2007 (130)
17 BCMHGSC_JDW ss93646319 Mar 24, 2008 (129)
18 HUMANGENOME_JCVI ss98139976 Feb 06, 2009 (130)
19 KRIBB_YJKIM ss104807673 Feb 06, 2009 (130)
20 BGI ss105507378 Feb 06, 2009 (130)
21 1000GENOMES ss111691937 Jan 25, 2009 (130)
22 1000GENOMES ss113478341 Jan 25, 2009 (130)
23 ILLUMINA-UK ss115987813 Feb 14, 2009 (130)
24 ENSEMBL ss142615178 Dec 01, 2009 (131)
25 ENSEMBL ss142760831 Dec 01, 2009 (131)
26 GMI ss154529330 Dec 01, 2009 (131)
27 COMPLETE_GENOMICS ss162141939 Jul 04, 2010 (132)
28 COMPLETE_GENOMICS ss163848459 Jul 04, 2010 (132)
29 COMPLETE_GENOMICS ss166295510 Jul 04, 2010 (132)
30 BUSHMAN ss203089906 Jul 04, 2010 (132)
31 BCM-HGSC-SUB ss207985539 Jul 04, 2010 (132)
32 1000GENOMES ss222968866 Jul 14, 2010 (132)
33 1000GENOMES ss233894614 Jul 15, 2010 (132)
34 1000GENOMES ss240866098 Jul 15, 2010 (132)
35 BL ss254128325 May 09, 2011 (134)
36 GMI ss279229232 May 04, 2012 (137)
37 GMI ss285592431 Apr 25, 2013 (138)
38 PJP ss294032328 May 09, 2011 (134)
39 ILLUMINA ss410908477 Sep 17, 2011 (135)
40 ILLUMINA ss480061642 May 04, 2012 (137)
41 ILLUMINA ss485409275 May 04, 2012 (137)
42 ILLUMINA ss533511966 Sep 08, 2015 (146)
43 TISHKOFF ss559875950 Apr 25, 2013 (138)
44 SSMP ss654229294 Apr 25, 2013 (138)
45 ILLUMINA ss779703252 Sep 08, 2015 (146)
46 ILLUMINA ss781137206 Sep 08, 2015 (146)
47 ILLUMINA ss835177439 Sep 08, 2015 (146)
48 EVA-GONL ss984064537 Aug 21, 2014 (142)
49 JMKIDD_LAB ss1074451686 Aug 21, 2014 (142)
50 1000GENOMES ss1324347710 Aug 21, 2014 (142)
51 DDI ss1431061346 Apr 01, 2015 (144)
52 EVA_GENOME_DK ss1582116844 Apr 01, 2015 (144)
53 EVA_DECODE ss1593633407 Apr 01, 2015 (144)
54 EVA_UK10K_ALSPAC ss1617795110 Apr 01, 2015 (144)
55 EVA_UK10K_TWINSUK ss1660789143 Apr 01, 2015 (144)
56 EVA_SVP ss1712939982 Apr 01, 2015 (144)
57 HAMMER_LAB ss1804916985 Sep 08, 2015 (146)
58 WEILL_CORNELL_DGM ss1927309530 Feb 12, 2016 (147)
59 GENOMED ss1970651700 Jul 19, 2016 (147)
60 JJLAB ss2024331932 Sep 14, 2016 (149)
61 USC_VALOUEV ss2152528012 Dec 20, 2016 (150)
62 HUMAN_LONGEVITY ss2292529503 Dec 20, 2016 (150)
63 TOPMED ss2461390317 Dec 20, 2016 (150)
64 SYSTEMSBIOZJU ss2626654888 Nov 08, 2017 (151)
65 ILLUMINA ss2634581346 Nov 08, 2017 (151)
66 GRF ss2708184837 Nov 08, 2017 (151)
67 GNOMAD ss2850933705 Nov 08, 2017 (151)
68 SWEGEN ss3000794775 Nov 08, 2017 (151)
69 BIOINF_KMB_FNS_UNIBA ss3025960236 Nov 08, 2017 (151)
70 CSHL ss3347488448 Nov 08, 2017 (151)
71 TOPMED ss3525184215 Nov 08, 2017 (151)
72 ILLUMINA ss3629774601 Oct 12, 2018 (152)
73 ILLUMINA ss3632490122 Oct 12, 2018 (152)
74 ILLUMINA ss3642551699 Oct 12, 2018 (152)
75 URBANLAB ss3648585887 Oct 12, 2018 (152)
76 EGCUT_WGS ss3668723597 Jul 13, 2019 (153)
77 EVA_DECODE ss3719305234 Jul 13, 2019 (153)
78 ACPOP ss3734452215 Jul 13, 2019 (153)
79 EVA ss3766317267 Jul 13, 2019 (153)
80 PACBIO ss3785760832 Jul 13, 2019 (153)
81 PACBIO ss3791071256 Jul 13, 2019 (153)
82 PACBIO ss3795951011 Jul 13, 2019 (153)
83 KHV_HUMAN_GENOMES ss3809484732 Jul 13, 2019 (153)
84 EVA ss3830470745 Apr 26, 2020 (154)
85 EVA ss3838722665 Apr 26, 2020 (154)
86 EVA ss3844173921 Apr 26, 2020 (154)
87 SGDP_PRJ ss3866854051 Apr 26, 2020 (154)
88 KRGDB ss3913892315 Apr 26, 2020 (154)
89 KOGIC ss3961078343 Apr 26, 2020 (154)
90 EVA ss3985283879 Apr 26, 2021 (155)
91 TOPMED ss4739193412 Apr 26, 2021 (155)
92 TOMMO_GENOMICS ss5182271161 Apr 26, 2021 (155)
93 1000Genomes NC_000007.13 - 25017962 Oct 12, 2018 (152)
94 The Avon Longitudinal Study of Parents and Children NC_000007.13 - 25017962 Oct 12, 2018 (152)
95 Genetic variation in the Estonian population NC_000007.13 - 25017962 Oct 12, 2018 (152)
96 The Danish reference pan genome NC_000007.13 - 25017962 Apr 26, 2020 (154)
97 gnomAD - Genomes NC_000007.14 - 24978343 Apr 26, 2021 (155)
98 Genome of the Netherlands Release 5 NC_000007.13 - 25017962 Apr 26, 2020 (154)
99 HapMap NC_000007.14 - 24978343 Apr 26, 2020 (154)
100 KOREAN population from KRGDB NC_000007.13 - 25017962 Apr 26, 2020 (154)
101 Korean Genome Project NC_000007.14 - 24978343 Apr 26, 2020 (154)
102 Northern Sweden NC_000007.13 - 25017962 Jul 13, 2019 (153)
103 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000007.13 - 25017962 Apr 26, 2021 (155)
104 Qatari NC_000007.13 - 25017962 Apr 26, 2020 (154)
105 SGDP_PRJ NC_000007.13 - 25017962 Apr 26, 2020 (154)
106 Siberian NC_000007.13 - 25017962 Apr 26, 2020 (154)
107 8.3KJPN NC_000007.13 - 25017962 Apr 26, 2021 (155)
108 TopMed NC_000007.14 - 24978343 Apr 26, 2021 (155)
109 UK 10K study - Twins NC_000007.13 - 25017962 Oct 12, 2018 (152)
110 A Vietnamese Genetic Variation Database NC_000007.13 - 25017962 Jul 13, 2019 (153)
111 ALFA NC_000007.14 - 24978343 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)
rs10369162 Feb 27, 2004 (120)
rs10429129 Feb 27, 2004 (120)
rs60722865 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
21069709, ss3913892315 NC_000007.13:25017961:C:G NC_000007.14:24978342:C:G (self)
ss78206681, ss81345663, ss82638472, ss84903580 NC_000007.11:24791201:C:T NC_000007.14:24978342:C:T (self)
ss93646319, ss111691937, ss113478341, ss115987813, ss162141939, ss163848459, ss166295510, ss203089906, ss207985539, ss254128325, ss279229232, ss285592431, ss294032328, ss485409275, ss1593633407, ss1712939982 NC_000007.12:24984486:C:T NC_000007.14:24978342:C:T (self)
36289732, 20231116, 14461845, 8281783, 9020182, 21069709, 7737080, 509806, 9351460, 18871031, 5044366, 40240468, 20231116, 4507806, ss222968866, ss233894614, ss240866098, ss480061642, ss533511966, ss559875950, ss654229294, ss779703252, ss781137206, ss835177439, ss984064537, ss1074451686, ss1324347710, ss1431061346, ss1582116844, ss1617795110, ss1660789143, ss1804916985, ss1927309530, ss1970651700, ss2024331932, ss2152528012, ss2461390317, ss2626654888, ss2634581346, ss2708184837, ss2850933705, ss3000794775, ss3347488448, ss3629774601, ss3632490122, ss3642551699, ss3668723597, ss3734452215, ss3766317267, ss3785760832, ss3791071256, ss3795951011, ss3830470745, ss3838722665, ss3866854051, ss3913892315, ss3985283879, ss5182271161 NC_000007.13:25017961:C:T NC_000007.14:24978342:C:T (self)
255883411, 3358939, 17456344, 360679495, 576570971, 5973783287, ss2292529503, ss3025960236, ss3525184215, ss3648585887, ss3719305234, ss3809484732, ss3844173921, ss3961078343, ss4739193412 NC_000007.14:24978342:C:T NC_000007.14:24978342:C:T (self)
ss10414866 NT_007819.13:24311569:C:T NC_000007.14:24978342:C:T (self)
ss14574621, ss14734392, ss17941371, ss19722158, ss20317745, ss22562848, ss22943051 NT_007819.14:24311569:C:T NC_000007.14:24978342:C:T (self)
ss158, ss3830883, ss6504381, ss76593613, ss98139976, ss104807673, ss105507378, ss142615178, ss142760831, ss154529330, ss410908477 NT_007819.17:25007961:C:T NC_000007.14:24978342:C:T (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 rs158
PMID Title Author Year Journal
24149050 ATHENA: the analysis tool for heritable and environmental network associations. Holzinger ER et al. 2014 Bioinformatics (Oxford, England)
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