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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.

rs12233987

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:39053445 (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
T>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.369307 (97752/264690, TOPMED)
C=0.379269 (53106/140022, GnomAD)
C=0.37023 (23736/64112, ALFA) (+ 19 more)
T=0.48938 (13829/28258, 14KJPN)
T=0.48496 (8128/16760, 8.3KJPN)
C=0.3646 (2335/6404, 1000G_30x)
C=0.3668 (1837/5008, 1000G)
C=0.4616 (2068/4480, Estonian)
C=0.4110 (1584/3854, ALSPAC)
C=0.4186 (1552/3708, TWINSUK)
T=0.4590 (1345/2930, KOREAN)
C=0.3508 (731/2084, HGDP_Stanford)
C=0.3832 (725/1892, HapMap)
T=0.4793 (878/1832, Korea1K)
C=0.408 (407/998, GoNL)
C=0.432 (259/600, NorthernSweden)
T=0.386 (122/316, SGDP_PRJ)
C=0.296 (64/216, Qatari)
C=0.390 (82/210, Vietnamese)
C=0.39 (34/88, Ancient Sardinia)
C=0.47 (19/40, GENOME_DK)
T=0.40 (16/40, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
RICTOR : Intron Variant
Publications
0 citations
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 64112 T=0.62977 C=0.37023, G=0.00000
European Sub 53810 T=0.60829 C=0.39171, G=0.00000
African Sub 3124 T=0.8431 C=0.1569, G=0.0000
African Others Sub 114 T=0.904 C=0.096, G=0.000
African American Sub 3010 T=0.8409 C=0.1591, G=0.0000
Asian Sub 112 T=0.670 C=0.330, G=0.000
East Asian Sub 76 T=0.62 C=0.38, G=0.00
Other Asian Sub 36 T=0.78 C=0.22, G=0.00
Latin American 1 Sub 168 T=0.750 C=0.250, G=0.000
Latin American 2 Sub 846 T=0.742 C=0.258, G=0.000
South Asian Sub 4890 T=0.6951 C=0.3049, G=0.0000
Other Sub 1162 T=0.6730 C=0.3270, G=0.0000


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 T=0.630693 C=0.369307
gnomAD - Genomes Global Study-wide 140022 T=0.620731 C=0.379269
gnomAD - Genomes European Sub 75852 T=0.58399 C=0.41601
gnomAD - Genomes African Sub 41934 T=0.70003 C=0.29997
gnomAD - Genomes American Sub 13642 T=0.61245 C=0.38755
gnomAD - Genomes Ashkenazi Jewish Sub 3322 T=0.5804 C=0.4196
gnomAD - Genomes East Asian Sub 3124 T=0.5269 C=0.4731
gnomAD - Genomes Other Sub 2148 T=0.6215 C=0.3785
Allele Frequency Aggregator Total Global 64112 T=0.62977 C=0.37023, G=0.00000
Allele Frequency Aggregator European Sub 53810 T=0.60829 C=0.39171, G=0.00000
Allele Frequency Aggregator South Asian Sub 4890 T=0.6951 C=0.3049, G=0.0000
Allele Frequency Aggregator African Sub 3124 T=0.8431 C=0.1569, G=0.0000
Allele Frequency Aggregator Other Sub 1162 T=0.6730 C=0.3270, G=0.0000
Allele Frequency Aggregator Latin American 2 Sub 846 T=0.742 C=0.258, G=0.000
Allele Frequency Aggregator Latin American 1 Sub 168 T=0.750 C=0.250, G=0.000
Allele Frequency Aggregator Asian Sub 112 T=0.670 C=0.330, G=0.000
14KJPN JAPANESE Study-wide 28258 T=0.48938 C=0.51062
8.3KJPN JAPANESE Study-wide 16760 T=0.48496 C=0.51504
1000Genomes_30x Global Study-wide 6404 T=0.6354 C=0.3646
1000Genomes_30x African Sub 1786 T=0.7318 C=0.2682
1000Genomes_30x Europe Sub 1266 T=0.5648 C=0.4352
1000Genomes_30x South Asian Sub 1202 T=0.6498 C=0.3502
1000Genomes_30x East Asian Sub 1170 T=0.5453 C=0.4547
1000Genomes_30x American Sub 980 T=0.641 C=0.359
1000Genomes Global Study-wide 5008 T=0.6332 C=0.3668
1000Genomes African Sub 1322 T=0.7262 C=0.2738
1000Genomes East Asian Sub 1008 T=0.5486 C=0.4514
1000Genomes Europe Sub 1006 T=0.5706 C=0.4294
1000Genomes South Asian Sub 978 T=0.654 C=0.346
1000Genomes American Sub 694 T=0.640 C=0.360
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.5384 C=0.4616
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.5890 C=0.4110
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.5814 C=0.4186
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.4590 C=0.5410
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 T=0.6492 C=0.3508
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.553 C=0.447
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 T=0.696 C=0.304
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 T=0.666 C=0.334
HGDP-CEPH-db Supplement 1 Europe Sub 320 T=0.625 C=0.375
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.719 C=0.281
HGDP-CEPH-db Supplement 1 America Sub 216 T=0.625 C=0.375
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.88 C=0.12
HapMap Global Study-wide 1892 T=0.6168 C=0.3832
HapMap American Sub 770 T=0.596 C=0.404
HapMap African Sub 692 T=0.708 C=0.292
HapMap Asian Sub 254 T=0.476 C=0.524
HapMap Europe Sub 176 T=0.551 C=0.449
Korean Genome Project KOREAN Study-wide 1832 T=0.4793 C=0.5207
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.592 C=0.408
Northern Sweden ACPOP Study-wide 600 T=0.568 C=0.432
SGDP_PRJ Global Study-wide 316 T=0.386 C=0.614
Qatari Global Study-wide 216 T=0.704 C=0.296
A Vietnamese Genetic Variation Database Global Study-wide 210 T=0.610 C=0.390
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 88 T=0.61 C=0.39
The Danish reference pan genome Danish Study-wide 40 T=0.53 C=0.47
Siberian Global Study-wide 40 T=0.40 C=0.60
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 5 NC_000005.10:g.39053445T>C
GRCh38.p14 chr 5 NC_000005.10:g.39053445T>G
GRCh37.p13 chr 5 NC_000005.9:g.39053547T>C
GRCh37.p13 chr 5 NC_000005.9:g.39053547T>G
Gene: RICTOR, RPTOR independent companion of MTOR complex 2 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
RICTOR transcript variant 2 NM_001285439.2:c.97+20666…

NM_001285439.2:c.97+20666A>G

N/A Intron Variant
RICTOR transcript variant 3 NM_001285440.2:c.-757+206…

NM_001285440.2:c.-757+20666A>G

N/A Intron Variant
RICTOR transcript variant 1 NM_152756.5:c.97+20666A>G N/A Intron Variant
RICTOR transcript variant X6 XM_006714463.4:c.97+20666…

XM_006714463.4:c.97+20666A>G

N/A Intron Variant
RICTOR transcript variant X2 XM_011514005.3:c.97+20666…

XM_011514005.3:c.97+20666A>G

N/A Intron Variant
RICTOR transcript variant X1 XM_017009311.2:c.49+20884…

XM_017009311.2:c.49+20884A>G

N/A Intron Variant
RICTOR transcript variant X3 XM_017009312.2:c.49+20884…

XM_017009312.2:c.49+20884A>G

N/A Intron Variant
RICTOR transcript variant X4 XM_047417068.1:c.-145+206…

XM_047417068.1:c.-145+20666A>G

N/A Intron Variant
RICTOR transcript variant X5 XM_047417069.1:c.49+20884…

XM_047417069.1:c.49+20884A>G

N/A Intron Variant
RICTOR transcript variant X8 XM_047417070.1:c.49+20884…

XM_047417070.1:c.49+20884A>G

N/A Intron Variant
RICTOR transcript variant X7 XM_011514006.4:c. N/A Genic Upstream Transcript 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 T= C G
GRCh38.p14 chr 5 NC_000005.10:g.39053445= NC_000005.10:g.39053445T>C NC_000005.10:g.39053445T>G
GRCh37.p13 chr 5 NC_000005.9:g.39053547= NC_000005.9:g.39053547T>C NC_000005.9:g.39053547T>G
RICTOR transcript variant 2 NM_001285439.2:c.97+20666= NM_001285439.2:c.97+20666A>G NM_001285439.2:c.97+20666A>C
RICTOR transcript variant 3 NM_001285440.2:c.-757+20666= NM_001285440.2:c.-757+20666A>G NM_001285440.2:c.-757+20666A>C
RICTOR transcript NM_152756.3:c.97+20666= NM_152756.3:c.97+20666A>G NM_152756.3:c.97+20666A>C
RICTOR transcript variant 1 NM_152756.5:c.97+20666= NM_152756.5:c.97+20666A>G NM_152756.5:c.97+20666A>C
RICTOR transcript variant X1 XM_005248277.1:c.97+20666= XM_005248277.1:c.97+20666A>G XM_005248277.1:c.97+20666A>C
RICTOR transcript variant X6 XM_006714463.4:c.97+20666= XM_006714463.4:c.97+20666A>G XM_006714463.4:c.97+20666A>C
RICTOR transcript variant X2 XM_011514005.3:c.97+20666= XM_011514005.3:c.97+20666A>G XM_011514005.3:c.97+20666A>C
RICTOR transcript variant X1 XM_017009311.2:c.49+20884= XM_017009311.2:c.49+20884A>G XM_017009311.2:c.49+20884A>C
RICTOR transcript variant X3 XM_017009312.2:c.49+20884= XM_017009312.2:c.49+20884A>G XM_017009312.2:c.49+20884A>C
RICTOR transcript variant X4 XM_047417068.1:c.-145+20666= XM_047417068.1:c.-145+20666A>G XM_047417068.1:c.-145+20666A>C
RICTOR transcript variant X5 XM_047417069.1:c.49+20884= XM_047417069.1:c.49+20884A>G XM_047417069.1:c.49+20884A>C
RICTOR transcript variant X8 XM_047417070.1:c.49+20884= XM_047417070.1:c.49+20884A>G XM_047417070.1:c.49+20884A>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#.

91 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_SNP ss18560774 Feb 28, 2004 (120)
2 SSAHASNP ss22333067 Apr 05, 2004 (121)
3 ABI ss42458839 Mar 14, 2006 (126)
4 ILLUMINA ss66992441 Dec 01, 2006 (127)
5 ILLUMINA ss67167658 Dec 01, 2006 (127)
6 ILLUMINA ss68124469 Dec 12, 2006 (127)
7 ILLUMINA ss70560832 May 27, 2008 (130)
8 ILLUMINA ss71098896 May 18, 2007 (127)
9 ILLUMINA ss75715200 Dec 05, 2007 (129)
10 KRIBB_YJKIM ss85199988 Dec 16, 2007 (130)
11 BCMHGSC_JDW ss93068091 Mar 24, 2008 (129)
12 HUMANGENOME_JCVI ss98613433 Feb 06, 2009 (130)
13 BGI ss105920324 Feb 06, 2009 (130)
14 1000GENOMES ss108974660 Jan 23, 2009 (130)
15 ENSEMBL ss143010680 Dec 01, 2009 (131)
16 ENSEMBL ss143057647 Dec 01, 2009 (131)
17 ILLUMINA ss153158805 Dec 01, 2009 (131)
18 GMI ss155328096 Dec 01, 2009 (131)
19 ILLUMINA ss159209286 Dec 01, 2009 (131)
20 COMPLETE_GENOMICS ss162190756 Jul 04, 2010 (132)
21 ILLUMINA ss171947767 Jul 04, 2010 (132)
22 BUSHMAN ss200140460 Jul 04, 2010 (132)
23 BCM-HGSC-SUB ss206947516 Jul 04, 2010 (132)
24 1000GENOMES ss221635074 Jul 14, 2010 (132)
25 1000GENOMES ss232912426 Jul 14, 2010 (132)
26 1000GENOMES ss240093509 Jul 15, 2010 (132)
27 GMI ss278253862 May 04, 2012 (137)
28 GMI ss285160140 Apr 25, 2013 (138)
29 PJP ss293571922 May 09, 2011 (134)
30 ILLUMINA ss536765468 Sep 08, 2015 (146)
31 TISHKOFF ss558338021 Apr 25, 2013 (138)
32 SSMP ss652193358 Apr 25, 2013 (138)
33 ILLUMINA ss832721703 Jul 13, 2019 (153)
34 EVA-GONL ss981467700 Aug 21, 2014 (142)
35 JMKIDD_LAB ss1072558830 Aug 21, 2014 (142)
36 1000GENOMES ss1314723928 Aug 21, 2014 (142)
37 DDI ss1430314263 Apr 01, 2015 (144)
38 EVA_GENOME_DK ss1581101472 Apr 01, 2015 (144)
39 EVA_DECODE ss1590990397 Apr 01, 2015 (144)
40 EVA_UK10K_ALSPAC ss1612697966 Apr 01, 2015 (144)
41 EVA_UK10K_TWINSUK ss1655691999 Apr 01, 2015 (144)
42 EVA_SVP ss1712758579 Apr 01, 2015 (144)
43 WEILL_CORNELL_DGM ss1924730321 Feb 12, 2016 (147)
44 GENOMED ss1970068645 Jul 19, 2016 (147)
45 JJLAB ss2022967930 Sep 14, 2016 (149)
46 USC_VALOUEV ss2151119034 Dec 20, 2016 (150)
47 HUMAN_LONGEVITY ss2273033532 Dec 20, 2016 (150)
48 SYSTEMSBIOZJU ss2625984525 Nov 08, 2017 (151)
49 GRF ss2706657187 Nov 08, 2017 (151)
50 GNOMAD ss2823488747 Nov 08, 2017 (151)
51 SWEGEN ss2996772282 Nov 08, 2017 (151)
52 BIOINF_KMB_FNS_UNIBA ss3025269374 Nov 08, 2017 (151)
53 CSHL ss3346344961 Nov 08, 2017 (151)
54 ILLUMINA ss3629219204 Oct 12, 2018 (152)
55 ILLUMINA ss3638549215 Oct 12, 2018 (152)
56 ILLUMINA ss3639277375 Oct 12, 2018 (152)
57 ILLUMINA ss3639936399 Oct 12, 2018 (152)
58 ILLUMINA ss3643495543 Oct 12, 2018 (152)
59 ILLUMINA ss3643982003 Oct 12, 2018 (152)
60 URBANLAB ss3648036550 Oct 12, 2018 (152)
61 EGCUT_WGS ss3664666492 Jul 13, 2019 (153)
62 EVA_DECODE ss3714508178 Jul 13, 2019 (153)
63 ACPOP ss3732275481 Jul 13, 2019 (153)
64 EVA ss3763319398 Jul 13, 2019 (153)
65 PACBIO ss3785087690 Jul 13, 2019 (153)
66 PACBIO ss3790497715 Jul 13, 2019 (153)
67 PACBIO ss3795374162 Jul 13, 2019 (153)
68 KHV_HUMAN_GENOMES ss3806495471 Jul 13, 2019 (153)
69 EVA ss3829203146 Apr 26, 2020 (154)
70 EVA ss3838070911 Apr 26, 2020 (154)
71 EVA ss3843510275 Apr 26, 2020 (154)
72 HGDP ss3847788149 Apr 26, 2020 (154)
73 SGDP_PRJ ss3861658268 Apr 26, 2020 (154)
74 KRGDB ss3908136301 Apr 26, 2020 (154)
75 KOGIC ss3956469044 Apr 26, 2020 (154)
76 EVA ss3985136501 Apr 26, 2021 (155)
77 EVA ss4017202958 Apr 26, 2021 (155)
78 TOPMED ss4656643083 Apr 26, 2021 (155)
79 TOMMO_GENOMICS ss5171309278 Apr 26, 2021 (155)
80 1000G_HIGH_COVERAGE ss5263610119 Oct 17, 2022 (156)
81 EVA ss5356968095 Oct 17, 2022 (156)
82 HUGCELL_USP ss5461871675 Oct 17, 2022 (156)
83 EVA ss5507986974 Oct 17, 2022 (156)
84 1000G_HIGH_COVERAGE ss5547054036 Oct 17, 2022 (156)
85 SANFORD_IMAGENETICS ss5637615718 Oct 17, 2022 (156)
86 TOMMO_GENOMICS ss5707237377 Oct 17, 2022 (156)
87 YY_MCH ss5806205358 Oct 17, 2022 (156)
88 EVA ss5834805059 Oct 17, 2022 (156)
89 EVA ss5854776152 Oct 17, 2022 (156)
90 EVA ss5893813555 Oct 17, 2022 (156)
91 EVA ss5966033465 Oct 17, 2022 (156)
92 1000Genomes NC_000005.9 - 39053547 Oct 12, 2018 (152)
93 1000Genomes_30x NC_000005.10 - 39053445 Oct 17, 2022 (156)
94 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 39053547 Oct 12, 2018 (152)
95 Genetic variation in the Estonian population NC_000005.9 - 39053547 Oct 12, 2018 (152)
96 The Danish reference pan genome NC_000005.9 - 39053547 Apr 26, 2020 (154)
97 gnomAD - Genomes NC_000005.10 - 39053445 Apr 26, 2021 (155)
98 Genome of the Netherlands Release 5 NC_000005.9 - 39053547 Apr 26, 2020 (154)
99 HGDP-CEPH-db Supplement 1 NC_000005.8 - 39089304 Apr 26, 2020 (154)
100 HapMap NC_000005.10 - 39053445 Apr 26, 2020 (154)
101 KOREAN population from KRGDB NC_000005.9 - 39053547 Apr 26, 2020 (154)
102 Korean Genome Project NC_000005.10 - 39053445 Apr 26, 2020 (154)
103 Northern Sweden NC_000005.9 - 39053547 Jul 13, 2019 (153)
104 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000005.9 - 39053547 Apr 26, 2021 (155)
105 Qatari NC_000005.9 - 39053547 Apr 26, 2020 (154)
106 SGDP_PRJ NC_000005.9 - 39053547 Apr 26, 2020 (154)
107 Siberian NC_000005.9 - 39053547 Apr 26, 2020 (154)
108 8.3KJPN NC_000005.9 - 39053547 Apr 26, 2021 (155)
109 14KJPN NC_000005.10 - 39053445 Oct 17, 2022 (156)
110 TopMed NC_000005.10 - 39053445 Apr 26, 2021 (155)
111 UK 10K study - Twins NC_000005.9 - 39053547 Oct 12, 2018 (152)
112 A Vietnamese Genetic Variation Database NC_000005.9 - 39053547 Jul 13, 2019 (153)
113 ALFA NC_000005.10 - 39053445 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)
rs61691121 May 27, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
466041, ss93068091, ss108974660, ss162190756, ss200140460, ss206947516, ss278253862, ss285160140, ss293571922, ss1590990397, ss1712758579, ss3639277375, ss3639936399, ss3643495543, ss3643982003, ss3847788149 NC_000005.8:39089303:T:C NC_000005.10:39053444:T:C (self)
26311272, 14632584, 10404740, 7266411, 6503079, 15313695, 5560346, 362428, 6772251, 13675248, 3635388, 29278585, 14632584, 3253338, ss221635074, ss232912426, ss240093509, ss536765468, ss558338021, ss652193358, ss832721703, ss981467700, ss1072558830, ss1314723928, ss1430314263, ss1581101472, ss1612697966, ss1655691999, ss1924730321, ss1970068645, ss2022967930, ss2151119034, ss2625984525, ss2706657187, ss2823488747, ss2996772282, ss3346344961, ss3629219204, ss3638549215, ss3664666492, ss3732275481, ss3763319398, ss3785087690, ss3790497715, ss3795374162, ss3829203146, ss3838070911, ss3861658268, ss3908136301, ss3985136501, ss4017202958, ss5171309278, ss5356968095, ss5507986974, ss5637615718, ss5834805059, ss5966033465 NC_000005.9:39053546:T:C NC_000005.10:39053444:T:C (self)
34579971, 185866522, 2850678, 12847045, 41074481, 494020640, 10890295050, ss2273033532, ss3025269374, ss3648036550, ss3714508178, ss3806495471, ss3843510275, ss3956469044, ss4656643083, ss5263610119, ss5461871675, ss5547054036, ss5707237377, ss5806205358, ss5854776152, ss5893813555 NC_000005.10:39053444:T:C NC_000005.10:39053444:T:C (self)
ss18560774, ss22333067 NT_006576.14:21505652:T:C NC_000005.10:39053444:T:C (self)
ss42458839, ss66992441, ss67167658, ss68124469, ss70560832, ss71098896, ss75715200, ss85199988, ss98613433, ss105920324, ss143010680, ss143057647, ss153158805, ss155328096, ss159209286, ss171947767 NT_006576.16:39043546:T:C NC_000005.10:39053444:T:C (self)
10890295050, ss2273033532 NC_000005.10:39053444:T:G NC_000005.10:39053444:T:G (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs12233987

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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
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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