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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.

rs124

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr7:24926377 (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
G>A / G>C / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.371574 (98352/264690, TOPMED)
G=0.381165 (53354/139976, GnomAD)
G=0.40201 (9629/23952, ALFA) (+ 16 more)
G=0.07925 (1328/16758, 8.3KJPN)
G=0.2696 (1350/5008, 1000G)
G=0.4308 (1930/4480, Estonian)
G=0.4538 (1749/3854, ALSPAC)
G=0.4312 (1599/3708, TWINSUK)
G=0.0870 (255/2930, KOREAN)
G=0.2742 (516/1882, HapMap)
G=0.0917 (168/1832, Korea1K)
G=0.450 (449/998, GoNL)
G=0.412 (247/600, NorthernSweden)
G=0.209 (103/494, SGDP_PRJ)
G=0.444 (96/216, Qatari)
G=0.061 (13/214, Vietnamese)
G=0.48 (26/54, Ancient Sardinia)
G=0.22 (11/50, Siberian)
G=0.42 (17/40, 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.24926377G>A
GRCh38.p13 chr 7 NC_000007.14:g.24926377G>C
GRCh38.p13 chr 7 NC_000007.14:g.24926377G>T
GRCh37.p13 chr 7 NC_000007.13:g.24965996G>A
GRCh37.p13 chr 7 NC_000007.13:g.24965996G>C
GRCh37.p13 chr 7 NC_000007.13:g.24965996G>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.-149-33756C…

NM_015550.4:c.-149-33756C>T

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.-149-337…

XM_006715681.3:c.-149-33756C>T

N/A Intron Variant
OSBPL3 transcript variant X4 XM_006715682.3:c.-149-337…

XM_006715682.3:c.-149-33756C>T

N/A Intron Variant
OSBPL3 transcript variant X7 XM_006715683.3:c.-149-337…

XM_006715683.3:c.-149-33756C>T

N/A Intron Variant
OSBPL3 transcript variant X15 XM_006715684.4:c.-1192-33…

XM_006715684.4:c.-1192-33756C>T

N/A Intron Variant
OSBPL3 transcript variant X5 XM_011515259.2:c.-628-337…

XM_011515259.2:c.-628-33756C>T

N/A Intron Variant
OSBPL3 transcript variant X6 XM_017011948.1:c.-491-337…

XM_017011948.1:c.-491-33756C>T

N/A Intron Variant
OSBPL3 transcript variant X8 XM_017011949.1:c.-628-337…

XM_017011949.1:c.-628-33756C>T

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 23952 G=0.40201 A=0.59799
European Sub 15664 G=0.44414 A=0.55586
African Sub 3618 G=0.2789 A=0.7211
African Others Sub 126 G=0.246 A=0.754
African American Sub 3492 G=0.2801 A=0.7199
Asian Sub 160 G=0.094 A=0.906
East Asian Sub 102 G=0.118 A=0.882
Other Asian Sub 58 G=0.05 A=0.95
Latin American 1 Sub 292 G=0.408 A=0.592
Latin American 2 Sub 2766 G=0.3670 A=0.6330
South Asian Sub 110 G=0.264 A=0.736
Other Sub 1342 G=0.3614 A=0.6386


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=0.371574 A=0.628426
gnomAD - Genomes Global Study-wide 139976 G=0.381165 A=0.618835
gnomAD - Genomes European Sub 75798 G=0.44989 A=0.55011
gnomAD - Genomes African Sub 41936 G=0.28057 A=0.71943
gnomAD - Genomes American Sub 13646 G=0.37161 A=0.62839
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.3898 A=0.6102
gnomAD - Genomes East Asian Sub 3134 G=0.0890 A=0.9110
gnomAD - Genomes Other Sub 2140 G=0.3935 A=0.6065
Allele Frequency Aggregator Total Global 23952 G=0.40201 A=0.59799
Allele Frequency Aggregator European Sub 15664 G=0.44414 A=0.55586
Allele Frequency Aggregator African Sub 3618 G=0.2789 A=0.7211
Allele Frequency Aggregator Latin American 2 Sub 2766 G=0.3670 A=0.6330
Allele Frequency Aggregator Other Sub 1342 G=0.3614 A=0.6386
Allele Frequency Aggregator Latin American 1 Sub 292 G=0.408 A=0.592
Allele Frequency Aggregator Asian Sub 160 G=0.094 A=0.906
Allele Frequency Aggregator South Asian Sub 110 G=0.264 A=0.736
8.3KJPN JAPANESE Study-wide 16758 G=0.07925 A=0.92075
1000Genomes Global Study-wide 5008 G=0.2696 A=0.7304
1000Genomes African Sub 1322 G=0.2587 A=0.7413
1000Genomes East Asian Sub 1008 G=0.0962 A=0.9038
1000Genomes Europe Sub 1006 G=0.4225 A=0.5775
1000Genomes South Asian Sub 978 G=0.256 A=0.744
1000Genomes American Sub 694 G=0.340 A=0.660
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.4308 A=0.5692
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.4538 A=0.5462
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.4312 A=0.5688
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.0870 A=0.9130, C=0.0000, T=0.0000
HapMap Global Study-wide 1882 G=0.2742 A=0.7258
HapMap American Sub 766 G=0.281 A=0.719
HapMap African Sub 688 G=0.283 A=0.717
HapMap Asian Sub 252 G=0.099 A=0.901
HapMap Europe Sub 176 G=0.460 A=0.540
Korean Genome Project KOREAN Study-wide 1832 G=0.0917 A=0.9083
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.450 A=0.550
Northern Sweden ACPOP Study-wide 600 G=0.412 A=0.588
SGDP_PRJ Global Study-wide 494 G=0.209 A=0.791
Qatari Global Study-wide 216 G=0.444 A=0.556
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.061 A=0.939
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 54 G=0.48 A=0.52
Siberian Global Study-wide 50 G=0.22 A=0.78
The Danish reference pan genome Danish Study-wide 40 G=0.42 A=0.57
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 C T
GRCh38.p13 chr 7 NC_000007.14:g.24926377= NC_000007.14:g.24926377G>A NC_000007.14:g.24926377G>C NC_000007.14:g.24926377G>T
GRCh37.p13 chr 7 NC_000007.13:g.24965996= NC_000007.13:g.24965996G>A NC_000007.13:g.24965996G>C NC_000007.13:g.24965996G>T
OSBPL3 transcript variant 1 NM_015550.2:c.-149-33756= NM_015550.2:c.-149-33756C>T NM_015550.2:c.-149-33756C>G NM_015550.2:c.-149-33756C>A
OSBPL3 transcript variant 1 NM_015550.4:c.-149-33756= NM_015550.4:c.-149-33756C>T NM_015550.4:c.-149-33756C>G NM_015550.4:c.-149-33756C>A
OSBPL3 transcript variant 2 NM_145320.1:c.-149-33756= NM_145320.1:c.-149-33756C>T NM_145320.1:c.-149-33756C>G NM_145320.1:c.-149-33756C>A
OSBPL3 transcript variant 3 NM_145321.1:c.-149-33756= NM_145321.1:c.-149-33756C>T NM_145321.1:c.-149-33756C>G NM_145321.1:c.-149-33756C>A
OSBPL3 transcript variant 4 NM_145322.1:c.-149-33756= NM_145322.1:c.-149-33756C>T NM_145322.1:c.-149-33756C>G NM_145322.1:c.-149-33756C>A
OSBPL3 transcript variant X3 XM_006715681.3:c.-149-33756= XM_006715681.3:c.-149-33756C>T XM_006715681.3:c.-149-33756C>G XM_006715681.3:c.-149-33756C>A
OSBPL3 transcript variant X4 XM_006715682.3:c.-149-33756= XM_006715682.3:c.-149-33756C>T XM_006715682.3:c.-149-33756C>G XM_006715682.3:c.-149-33756C>A
OSBPL3 transcript variant X7 XM_006715683.3:c.-149-33756= XM_006715683.3:c.-149-33756C>T XM_006715683.3:c.-149-33756C>G XM_006715683.3:c.-149-33756C>A
OSBPL3 transcript variant X15 XM_006715684.4:c.-1192-33756= XM_006715684.4:c.-1192-33756C>T XM_006715684.4:c.-1192-33756C>G XM_006715684.4:c.-1192-33756C>A
OSBPL3 transcript variant X5 XM_011515259.2:c.-628-33756= XM_011515259.2:c.-628-33756C>T XM_011515259.2:c.-628-33756C>G XM_011515259.2:c.-628-33756C>A
OSBPL3 transcript variant X6 XM_017011948.1:c.-491-33756= XM_017011948.1:c.-491-33756C>T XM_017011948.1:c.-491-33756C>G XM_017011948.1:c.-491-33756C>A
OSBPL3 transcript variant X8 XM_017011949.1:c.-628-33756= XM_017011949.1:c.-628-33756C>T XM_017011949.1:c.-628-33756C>G XM_017011949.1:c.-628-33756C>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#.

71 SubSNP, 19 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss124 Sep 19, 2000 (36)
2 TSC-CSHL ss1307064 Oct 05, 2000 (92)
3 SC_JCM ss6253636 Feb 20, 2003 (111)
4 BCM_SSAHASNP ss10403894 Jul 11, 2003 (116)
5 CSHL-HAPMAP ss17177821 Feb 27, 2004 (120)
6 CSHL-HAPMAP ss19719139 Feb 27, 2004 (120)
7 CSHL-HAPMAP ss20315353 Feb 27, 2004 (120)
8 ABI ss43060588 Mar 14, 2006 (126)
9 AFFY ss76823887 Dec 07, 2007 (129)
10 HGSV ss78727256 Dec 07, 2007 (129)
11 BCMHGSC_JDW ss93646267 Mar 24, 2008 (129)
12 HUMANGENOME_JCVI ss98241043 Feb 06, 2009 (130)
13 BGI ss104410170 Dec 01, 2009 (131)
14 KRIBB_YJKIM ss104807671 Feb 06, 2009 (130)
15 1000GENOMES ss111691247 Jan 25, 2009 (130)
16 1000GENOMES ss113477719 Jan 25, 2009 (130)
17 ILLUMINA-UK ss115987656 Feb 14, 2009 (130)
18 ENSEMBL ss142760444 Dec 01, 2009 (131)
19 ENSEMBL ss143543213 Dec 01, 2009 (131)
20 GMI ss154529022 Dec 01, 2009 (131)
21 COMPLETE_GENOMICS ss163847589 Jul 04, 2010 (132)
22 COMPLETE_GENOMICS ss166295027 Jul 04, 2010 (132)
23 BUSHMAN ss203089436 Jul 04, 2010 (132)
24 BCM-HGSC-SUB ss208231226 Jul 04, 2010 (132)
25 1000GENOMES ss222968640 Jul 14, 2010 (132)
26 1000GENOMES ss233894433 Jul 15, 2010 (132)
27 1000GENOMES ss240865973 Jul 15, 2010 (132)
28 BL ss254128129 May 09, 2011 (134)
29 GMI ss279229096 May 04, 2012 (137)
30 GMI ss285592356 Apr 25, 2013 (138)
31 PJP ss294032253 May 09, 2011 (134)
32 TISHKOFF ss559875703 Apr 25, 2013 (138)
33 SSMP ss654229022 Apr 25, 2013 (138)
34 EVA-GONL ss984064104 Aug 21, 2014 (142)
35 JMKIDD_LAB ss1074451402 Aug 21, 2014 (142)
36 1000GENOMES ss1324346246 Aug 21, 2014 (142)
37 DDI ss1431061210 Apr 01, 2015 (144)
38 EVA_GENOME_DK ss1582116660 Apr 01, 2015 (144)
39 EVA_DECODE ss1593632969 Apr 01, 2015 (144)
40 EVA_UK10K_ALSPAC ss1617794271 Apr 01, 2015 (144)
41 EVA_UK10K_TWINSUK ss1660788304 Apr 01, 2015 (144)
42 EVA_SVP ss1712939940 Apr 01, 2015 (144)
43 HAMMER_LAB ss1804916811 Sep 08, 2015 (146)
44 WEILL_CORNELL_DGM ss1927309163 Feb 12, 2016 (147)
45 GENOMED ss1970651585 Jul 19, 2016 (147)
46 JJLAB ss2024331657 Sep 14, 2016 (149)
47 USC_VALOUEV ss2152527805 Dec 20, 2016 (150)
48 HUMAN_LONGEVITY ss2292526379 Dec 20, 2016 (150)
49 TOPMED ss2461387133 Dec 20, 2016 (150)
50 SYSTEMSBIOZJU ss2626654782 Nov 08, 2017 (151)
51 GRF ss2708184636 Nov 08, 2017 (151)
52 GNOMAD ss2850929627 Nov 08, 2017 (151)
53 SWEGEN ss3000794182 Nov 08, 2017 (151)
54 BIOINF_KMB_FNS_UNIBA ss3025960125 Nov 08, 2017 (151)
55 CSHL ss3347488279 Nov 08, 2017 (151)
56 TOPMED ss3525174861 Nov 08, 2017 (151)
57 URBANLAB ss3648585792 Oct 12, 2018 (152)
58 EGCUT_WGS ss3668722956 Jul 13, 2019 (153)
59 EVA_DECODE ss3719304472 Jul 13, 2019 (153)
60 ACPOP ss3734451870 Jul 13, 2019 (153)
61 EVA ss3766316816 Jul 13, 2019 (153)
62 KHV_HUMAN_GENOMES ss3809484251 Jul 13, 2019 (153)
63 EVA ss3830470562 Apr 26, 2020 (154)
64 EVA ss3838722550 Apr 26, 2020 (154)
65 EVA ss3844173806 Apr 26, 2020 (154)
66 SGDP_PRJ ss3866853270 Apr 26, 2020 (154)
67 KRGDB ss3913891571 Apr 26, 2020 (154)
68 KOGIC ss3961077705 Apr 26, 2020 (154)
69 EVA ss3985283843 Apr 26, 2021 (155)
70 TOPMED ss4739180556 Apr 26, 2021 (155)
71 TOMMO_GENOMICS ss5182269650 Apr 26, 2021 (155)
72 1000Genomes NC_000007.13 - 24965996 Oct 12, 2018 (152)
73 The Avon Longitudinal Study of Parents and Children NC_000007.13 - 24965996 Oct 12, 2018 (152)
74 Genetic variation in the Estonian population NC_000007.13 - 24965996 Oct 12, 2018 (152)
75 The Danish reference pan genome NC_000007.13 - 24965996 Apr 26, 2020 (154)
76 gnomAD - Genomes NC_000007.14 - 24926377 Apr 26, 2021 (155)
77 Genome of the Netherlands Release 5 NC_000007.13 - 24965996 Apr 26, 2020 (154)
78 HapMap NC_000007.14 - 24926377 Apr 26, 2020 (154)
79 KOREAN population from KRGDB NC_000007.13 - 24965996 Apr 26, 2020 (154)
80 Korean Genome Project NC_000007.14 - 24926377 Apr 26, 2020 (154)
81 Northern Sweden NC_000007.13 - 24965996 Jul 13, 2019 (153)
82 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000007.13 - 24965996 Apr 26, 2021 (155)
83 Qatari NC_000007.13 - 24965996 Apr 26, 2020 (154)
84 SGDP_PRJ NC_000007.13 - 24965996 Apr 26, 2020 (154)
85 Siberian NC_000007.13 - 24965996 Apr 26, 2020 (154)
86 8.3KJPN NC_000007.13 - 24965996 Apr 26, 2021 (155)
87 TopMed NC_000007.14 - 24926377 Apr 26, 2021 (155)
88 UK 10K study - Twins NC_000007.13 - 24965996 Oct 12, 2018 (152)
89 A Vietnamese Genetic Variation Database NC_000007.13 - 24965996 Jul 13, 2019 (153)
90 ALFA NC_000007.14 - 24926377 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)
rs880779 Jan 18, 2001 (92)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss78727256 NC_000007.11:24739235:G:A NC_000007.14:24926376:G:A (self)
ss76823887, ss93646267, ss111691247, ss113477719, ss115987656, ss163847589, ss166295027, ss203089436, ss208231226, ss254128129, ss279229096, ss285592356, ss294032253, ss1593632969, ss1712939940 NC_000007.12:24932520:G:A NC_000007.14:24926376:G:A (self)
36288211, 20230192, 14461204, 8281599, 9019750, 21068965, 7736735, 509770, 9351093, 18870250, 5044159, 40238957, 20230192, 4507598, ss222968640, ss233894433, ss240865973, ss559875703, ss654229022, ss984064104, ss1074451402, ss1324346246, ss1431061210, ss1582116660, ss1617794271, ss1660788304, ss1804916811, ss1927309163, ss1970651585, ss2024331657, ss2152527805, ss2461387133, ss2626654782, ss2708184636, ss2850929627, ss3000794182, ss3347488279, ss3668722956, ss3734451870, ss3766316816, ss3830470562, ss3838722550, ss3866853270, ss3913891571, ss3985283843, ss5182269650 NC_000007.13:24965995:G:A NC_000007.14:24926376:G:A (self)
255873233, 3358840, 17455706, 360671328, 576558115, 176505090, ss2292526379, ss3025960125, ss3525174861, ss3648585792, ss3719304472, ss3809484251, ss3844173806, ss3961077705, ss4739180556 NC_000007.14:24926376:G:A NC_000007.14:24926376:G:A (self)
ss10403894 NT_007819.13:24259603:G:A NC_000007.14:24926376:G:A (self)
ss17177821, ss19719139, ss20315353 NT_007819.14:24259603:G:A NC_000007.14:24926376:G:A (self)
ss124, ss1307064, ss6253636, ss43060588, ss98241043, ss104410170, ss104807671, ss142760444, ss143543213, ss154529022 NT_007819.17:24955995:G:A NC_000007.14:24926376:G:A (self)
21068965, ss3913891571 NC_000007.13:24965995:G:C NC_000007.14:24926376:G:C (self)
21068965, ss3913891571 NC_000007.13:24965995:G:T NC_000007.14:24926376:G:T (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 rs124

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