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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.

rs1466113

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr17:73169179 (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
C>G / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.347947 (92098/264690, TOPMED)
C=0.38991 (11018/28258, 14KJPN)
C=0.39576 (6633/16760, 8.3KJPN) (+ 20 more)
C=0.4872 (4701/9650, ALFA)
C=0.3154 (2020/6404, 1000G_30x)
C=0.3171 (1588/5008, 1000G)
C=0.4069 (1823/4480, Estonian)
C=0.4354 (1678/3854, ALSPAC)
C=0.4285 (1589/3708, TWINSUK)
C=0.4577 (1341/2930, KOREAN)
C=0.2989 (565/1890, HapMap)
C=0.4165 (763/1832, Korea1K)
C=0.3336 (365/1094, Daghestan)
C=0.429 (428/998, GoNL)
C=0.466 (369/792, PRJEB37584)
C=0.432 (259/600, NorthernSweden)
C=0.466 (249/534, MGP)
C=0.224 (107/478, SGDP_PRJ)
C=0.361 (78/216, Qatari)
C=0.411 (88/214, Vietnamese)
C=0.40 (36/90, Ancient Sardinia)
C=0.31 (16/52, Siberian)
C=0.40 (16/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SSTR2 : Intron Variant
Publications
3 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 9650 C=0.4872 G=0.5128, T=0.0000
European Sub 8472 C=0.4907 G=0.5093, T=0.0000
African Sub 778 C=0.364 G=0.636, T=0.000
African Others Sub 32 C=0.22 G=0.78, T=0.00
African American Sub 746 C=0.370 G=0.630, T=0.000
Asian Sub 28 C=0.96 G=0.04, T=0.00
East Asian Sub 20 C=1.00 G=0.00, T=0.00
Other Asian Sub 8 C=0.9 G=0.1, T=0.0
Latin American 1 Sub 24 C=1.00 G=0.00, T=0.00
Latin American 2 Sub 52 C=1.00 G=0.00, T=0.00
South Asian Sub 10 C=0.8 G=0.2, T=0.0
Other Sub 286 C=0.524 G=0.476, T=0.000


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=0.347947 G=0.652053
14KJPN JAPANESE Study-wide 28258 C=0.38991 G=0.61009
8.3KJPN JAPANESE Study-wide 16760 C=0.39576 G=0.60424
Allele Frequency Aggregator Total Global 9650 C=0.4872 G=0.5128, T=0.0000
Allele Frequency Aggregator European Sub 8472 C=0.4907 G=0.5093, T=0.0000
Allele Frequency Aggregator African Sub 778 C=0.364 G=0.636, T=0.000
Allele Frequency Aggregator Other Sub 286 C=0.524 G=0.476, T=0.000
Allele Frequency Aggregator Latin American 2 Sub 52 C=1.00 G=0.00, T=0.00
Allele Frequency Aggregator Asian Sub 28 C=0.96 G=0.04, T=0.00
Allele Frequency Aggregator Latin American 1 Sub 24 C=1.00 G=0.00, T=0.00
Allele Frequency Aggregator South Asian Sub 10 C=0.8 G=0.2, T=0.0
1000Genomes_30x Global Study-wide 6404 C=0.3154 G=0.6846
1000Genomes_30x African Sub 1786 C=0.2016 G=0.7984
1000Genomes_30x Europe Sub 1266 C=0.3807 G=0.6193
1000Genomes_30x South Asian Sub 1202 C=0.2787 G=0.7213
1000Genomes_30x East Asian Sub 1170 C=0.4444 G=0.5556
1000Genomes_30x American Sub 980 C=0.330 G=0.670
1000Genomes Global Study-wide 5008 C=0.3171 G=0.6829
1000Genomes African Sub 1322 C=0.2035 G=0.7965
1000Genomes East Asian Sub 1008 C=0.4345 G=0.5655
1000Genomes Europe Sub 1006 C=0.3728 G=0.6272
1000Genomes South Asian Sub 978 C=0.279 G=0.721
1000Genomes American Sub 694 C=0.336 G=0.664
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.4069 G=0.5931
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.4354 G=0.5646
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.4285 G=0.5715
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.4577 G=0.5423
HapMap Global Study-wide 1890 C=0.2989 G=0.7011
HapMap American Sub 770 C=0.347 G=0.653
HapMap African Sub 690 C=0.194 G=0.806
HapMap Asian Sub 254 C=0.398 G=0.602
HapMap Europe Sub 176 C=0.358 G=0.642
Korean Genome Project KOREAN Study-wide 1832 C=0.4165 G=0.5835
Genome-wide autozygosity in Daghestan Global Study-wide 1094 C=0.3336 G=0.6664
Genome-wide autozygosity in Daghestan Daghestan Sub 612 C=0.291 G=0.709
Genome-wide autozygosity in Daghestan Near_East Sub 136 C=0.449 G=0.551
Genome-wide autozygosity in Daghestan Central Asia Sub 122 C=0.426 G=0.574
Genome-wide autozygosity in Daghestan Europe Sub 102 C=0.353 G=0.647
Genome-wide autozygosity in Daghestan South Asian Sub 88 C=0.32 G=0.68
Genome-wide autozygosity in Daghestan Caucasus Sub 34 C=0.29 G=0.71
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.429 G=0.571
CNV burdens in cranial meningiomas Global Study-wide 792 C=0.466 G=0.534
CNV burdens in cranial meningiomas CRM Sub 792 C=0.466 G=0.534
Northern Sweden ACPOP Study-wide 600 C=0.432 G=0.568
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 C=0.466 G=0.534
SGDP_PRJ Global Study-wide 478 C=0.224 G=0.776
Qatari Global Study-wide 216 C=0.361 G=0.639
A Vietnamese Genetic Variation Database Global Study-wide 214 C=0.411 G=0.589
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 90 C=0.40 G=0.60
Siberian Global Study-wide 52 C=0.31 G=0.69
The Danish reference pan genome Danish Study-wide 40 C=0.40 G=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 17 NC_000017.11:g.73169179C>G
GRCh38.p14 chr 17 NC_000017.11:g.73169179C>T
GRCh37.p13 chr 17 NC_000017.10:g.71165318C>G
GRCh37.p13 chr 17 NC_000017.10:g.71165318C>T
SSTR2 RefSeqGene NG_029371.1:g.9159C>G
SSTR2 RefSeqGene NG_029371.1:g.9159C>T
Gene: SSTR2, somatostatin receptor 2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SSTR2 transcript NM_001050.3:c.-92-49C>G 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 C= G T
GRCh38.p14 chr 17 NC_000017.11:g.73169179= NC_000017.11:g.73169179C>G NC_000017.11:g.73169179C>T
GRCh37.p13 chr 17 NC_000017.10:g.71165318= NC_000017.10:g.71165318C>G NC_000017.10:g.71165318C>T
SSTR2 RefSeqGene NG_029371.1:g.9159= NG_029371.1:g.9159C>G NG_029371.1:g.9159C>T
SSTR2 transcript NM_001050.2:c.-92-49= NM_001050.2:c.-92-49C>G NM_001050.2:c.-92-49C>T
SSTR2 transcript NM_001050.3:c.-92-49= NM_001050.3:c.-92-49C>G NM_001050.3:c.-92-49C>T
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#.

112 SubSNP, 25 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss2286476 Oct 23, 2000 (88)
2 SC_JCM ss5694736 Feb 20, 2003 (111)
3 SNP500CANCER ss8819902 Jul 02, 2003 (116)
4 BCM_SSAHASNP ss10858930 Jul 11, 2003 (116)
5 CSHL-HAPMAP ss16737721 Feb 27, 2004 (120)
6 SSAHASNP ss21433259 Apr 05, 2004 (121)
7 PERLEGEN ss24214907 Sep 20, 2004 (123)
8 ABI ss44036681 Mar 14, 2006 (126)
9 ILLUMINA ss65748517 Oct 16, 2006 (127)
10 AFFY ss65941421 Dec 01, 2006 (127)
11 AFFY ss66222682 Dec 01, 2006 (127)
12 PERLEGEN ss69201921 May 17, 2007 (127)
13 AFFY ss76369039 Dec 07, 2007 (129)
14 HGSV ss80475951 Dec 15, 2007 (130)
15 KRIBB_YJKIM ss81496866 Dec 15, 2007 (130)
16 HGSV ss83939076 Dec 15, 2007 (130)
17 HGSV ss84792973 Dec 15, 2007 (130)
18 HGSV ss85773680 Dec 15, 2007 (130)
19 BCMHGSC_JDW ss90655873 Mar 24, 2008 (129)
20 HUMANGENOME_JCVI ss96609993 Feb 06, 2009 (130)
21 1000GENOMES ss109908514 Jan 24, 2009 (130)
22 1000GENOMES ss113814725 Jan 25, 2009 (130)
23 ILLUMINA-UK ss118122226 Feb 14, 2009 (130)
24 ENSEMBL ss132637158 Dec 01, 2009 (131)
25 ENSEMBL ss137176656 Dec 01, 2009 (131)
26 COMPLETE_GENOMICS ss168478328 Jul 04, 2010 (132)
27 COMPLETE_GENOMICS ss170175355 Jul 04, 2010 (132)
28 COMPLETE_GENOMICS ss171707932 Jul 04, 2010 (132)
29 ILLUMINA ss172523018 Jul 04, 2010 (132)
30 AFFY ss173400326 Jul 04, 2010 (132)
31 BUSHMAN ss202763781 Jul 04, 2010 (132)
32 BCM-HGSC-SUB ss207814868 Jul 04, 2010 (132)
33 1000GENOMES ss227649010 Jul 14, 2010 (132)
34 1000GENOMES ss237316527 Jul 15, 2010 (132)
35 1000GENOMES ss243596138 Jul 15, 2010 (132)
36 ILLUMINA ss244279640 Jul 04, 2010 (132)
37 BL ss255781736 May 09, 2011 (134)
38 GMI ss282836825 May 04, 2012 (137)
39 GMI ss287213307 Apr 25, 2013 (138)
40 PJP ss291991210 May 09, 2011 (134)
41 ILLUMINA ss479734263 May 04, 2012 (137)
42 ILLUMINA ss483666814 May 04, 2012 (137)
43 ILLUMINA ss533235522 Sep 08, 2015 (146)
44 TISHKOFF ss565396154 Apr 25, 2013 (138)
45 SSMP ss661208724 Apr 25, 2013 (138)
46 ILLUMINA ss779641920 Aug 21, 2014 (142)
47 ILLUMINA ss781055289 Aug 21, 2014 (142)
48 ILLUMINA ss835114766 Aug 21, 2014 (142)
49 EVA-GONL ss993318142 Aug 21, 2014 (142)
50 JMKIDD_LAB ss1081204536 Aug 21, 2014 (142)
51 1000GENOMES ss1359480920 Aug 21, 2014 (142)
52 HAMMER_LAB ss1397735205 Sep 08, 2015 (146)
53 DDI ss1428092451 Apr 01, 2015 (144)
54 EVA_GENOME_DK ss1578238098 Apr 01, 2015 (144)
55 EVA_UK10K_ALSPAC ss1636074436 Apr 01, 2015 (144)
56 EVA_UK10K_TWINSUK ss1679068469 Apr 01, 2015 (144)
57 EVA_DECODE ss1697368422 Apr 01, 2015 (144)
58 EVA_MGP ss1711471238 Apr 01, 2015 (144)
59 EVA_SVP ss1713597267 Apr 01, 2015 (144)
60 HAMMER_LAB ss1808874188 Sep 08, 2015 (146)
61 WEILL_CORNELL_DGM ss1936779808 Feb 12, 2016 (147)
62 GENOMED ss1968432296 Jul 19, 2016 (147)
63 JJLAB ss2029162614 Sep 14, 2016 (149)
64 USC_VALOUEV ss2157646699 Dec 20, 2016 (150)
65 HUMAN_LONGEVITY ss2218497005 Dec 20, 2016 (150)
66 SYSTEMSBIOZJU ss2629076060 Nov 08, 2017 (151)
67 ILLUMINA ss2633422084 Nov 08, 2017 (151)
68 GRF ss2702212754 Nov 08, 2017 (151)
69 GNOMAD ss2952292734 Nov 08, 2017 (151)
70 AFFY ss2985740573 Nov 08, 2017 (151)
71 SWEGEN ss3015876480 Nov 08, 2017 (151)
72 BIOINF_KMB_FNS_UNIBA ss3028403918 Nov 08, 2017 (151)
73 CSHL ss3351833228 Nov 08, 2017 (151)
74 ILLUMINA ss3627717597 Oct 12, 2018 (152)
75 ILLUMINA ss3631401733 Oct 12, 2018 (152)
76 ILLUMINA ss3638174014 Oct 12, 2018 (152)
77 ILLUMINA ss3642004193 Oct 12, 2018 (152)
78 URBANLAB ss3650698487 Oct 12, 2018 (152)
79 EGCUT_WGS ss3682741951 Jul 13, 2019 (153)
80 EVA_DECODE ss3700882142 Jul 13, 2019 (153)
81 ACPOP ss3742202190 Jul 13, 2019 (153)
82 EVA ss3754913102 Jul 13, 2019 (153)
83 PACBIO ss3788263495 Jul 13, 2019 (153)
84 PACBIO ss3793209652 Jul 13, 2019 (153)
85 PACBIO ss3798095658 Jul 13, 2019 (153)
86 KHV_HUMAN_GENOMES ss3820179242 Jul 13, 2019 (153)
87 EVA ss3834969501 Apr 27, 2020 (154)
88 EVA ss3841096985 Apr 27, 2020 (154)
89 EVA ss3846595172 Apr 27, 2020 (154)
90 SGDP_PRJ ss3886182489 Apr 27, 2020 (154)
91 KRGDB ss3935951411 Apr 27, 2020 (154)
92 KOGIC ss3979254105 Apr 27, 2020 (154)
93 FSA-LAB ss3984122252 Apr 27, 2021 (155)
94 EVA ss3984726375 Apr 27, 2021 (155)
95 EVA ss3985802630 Apr 27, 2021 (155)
96 TOPMED ss5043327011 Apr 27, 2021 (155)
97 TOMMO_GENOMICS ss5223404775 Apr 27, 2021 (155)
98 EVA ss5237240505 Apr 27, 2021 (155)
99 1000G_HIGH_COVERAGE ss5303878177 Oct 16, 2022 (156)
100 EVA ss5315901049 Oct 16, 2022 (156)
101 HUGCELL_USP ss5496848215 Oct 16, 2022 (156)
102 1000G_HIGH_COVERAGE ss5607954872 Oct 16, 2022 (156)
103 EVA ss5624075386 Oct 16, 2022 (156)
104 SANFORD_IMAGENETICS ss5660511104 Oct 16, 2022 (156)
105 TOMMO_GENOMICS ss5779925497 Oct 16, 2022 (156)
106 EVA ss5800211115 Oct 16, 2022 (156)
107 YY_MCH ss5816714122 Oct 16, 2022 (156)
108 EVA ss5834264842 Oct 16, 2022 (156)
109 EVA ss5851889474 Oct 16, 2022 (156)
110 EVA ss5914764026 Oct 16, 2022 (156)
111 EVA ss5951913168 Oct 16, 2022 (156)
112 EVA ss5980981460 Oct 16, 2022 (156)
113 1000Genomes NC_000017.10 - 71165318 Oct 12, 2018 (152)
114 1000Genomes_30x NC_000017.11 - 73169179 Oct 16, 2022 (156)
115 The Avon Longitudinal Study of Parents and Children NC_000017.10 - 71165318 Oct 12, 2018 (152)
116 Genome-wide autozygosity in Daghestan NC_000017.9 - 68676913 Apr 27, 2020 (154)
117 Genetic variation in the Estonian population NC_000017.10 - 71165318 Oct 12, 2018 (152)
118 The Danish reference pan genome NC_000017.10 - 71165318 Apr 27, 2020 (154)
119 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 513439487 (NC_000017.11:73169178:C:G 89508/140056)
Row 513439488 (NC_000017.11:73169178:C:T 1/140136)

- Apr 27, 2021 (155)
120 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 513439487 (NC_000017.11:73169178:C:G 89508/140056)
Row 513439488 (NC_000017.11:73169178:C:T 1/140136)

- Apr 27, 2021 (155)
121 Genome of the Netherlands Release 5 NC_000017.10 - 71165318 Apr 27, 2020 (154)
122 HapMap NC_000017.11 - 73169179 Apr 27, 2020 (154)
123 KOREAN population from KRGDB NC_000017.10 - 71165318 Apr 27, 2020 (154)
124 Korean Genome Project NC_000017.11 - 73169179 Apr 27, 2020 (154)
125 Medical Genome Project healthy controls from Spanish population NC_000017.10 - 71165318 Apr 27, 2020 (154)
126 Northern Sweden NC_000017.10 - 71165318 Jul 13, 2019 (153)
127 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000017.10 - 71165318 Apr 27, 2021 (155)
128 CNV burdens in cranial meningiomas NC_000017.10 - 71165318 Apr 27, 2021 (155)
129 Qatari NC_000017.10 - 71165318 Apr 27, 2020 (154)
130 SGDP_PRJ NC_000017.10 - 71165318 Apr 27, 2020 (154)
131 Siberian NC_000017.10 - 71165318 Apr 27, 2020 (154)
132 8.3KJPN NC_000017.10 - 71165318 Apr 27, 2021 (155)
133 14KJPN NC_000017.11 - 73169179 Oct 16, 2022 (156)
134 TopMed NC_000017.11 - 73169179 Apr 27, 2021 (155)
135 UK 10K study - Twins NC_000017.10 - 71165318 Oct 12, 2018 (152)
136 A Vietnamese Genetic Variation Database NC_000017.10 - 71165318 Jul 13, 2019 (153)
137 ALFA NC_000017.11 - 73169179 Apr 27, 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)
rs17248470 Oct 08, 2004 (123)
rs59349722 Feb 27, 2009 (130)
rs60080728 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
205025, ss66222682, ss76369039, ss80475951, ss83939076, ss84792973, ss85773680, ss90655873, ss109908514, ss113814725, ss118122226, ss168478328, ss170175355, ss171707932, ss173400326, ss202763781, ss207814868, ss255781736, ss282836825, ss287213307, ss291991210, ss483666814, ss1397735205, ss1697368422, ss1713597267 NC_000017.9:68676912:C:G NC_000017.11:73169178:C:G (self)
72754815, 40316980, 28480199, 4437019, 17961854, 43128805, 586998, 15487055, 1028557, 275923, 18821730, 38199469, 10163053, 81374082, 40316980, 8912068, ss227649010, ss237316527, ss243596138, ss479734263, ss533235522, ss565396154, ss661208724, ss779641920, ss781055289, ss835114766, ss993318142, ss1081204536, ss1359480920, ss1428092451, ss1578238098, ss1636074436, ss1679068469, ss1711471238, ss1808874188, ss1936779808, ss1968432296, ss2029162614, ss2157646699, ss2629076060, ss2633422084, ss2702212754, ss2952292734, ss2985740573, ss3015876480, ss3351833228, ss3627717597, ss3631401733, ss3638174014, ss3642004193, ss3682741951, ss3742202190, ss3754913102, ss3788263495, ss3793209652, ss3798095658, ss3834969501, ss3841096985, ss3886182489, ss3935951411, ss3984122252, ss3984726375, ss3985802630, ss5223404775, ss5315901049, ss5624075386, ss5660511104, ss5800211115, ss5834264842, ss5951913168, ss5980981460 NC_000017.10:71165317:C:G NC_000017.11:73169178:C:G (self)
95480807, 1524901, 35632106, 113762601, 258872673, 13646875960, ss2218497005, ss3028403918, ss3650698487, ss3700882142, ss3820179242, ss3846595172, ss3979254105, ss5043327011, ss5237240505, ss5303878177, ss5496848215, ss5607954872, ss5779925497, ss5816714122, ss5851889474, ss5914764026 NC_000017.11:73169178:C:G NC_000017.11:73169178:C:G (self)
ss10858930 NT_010641.13:5057478:C:G NC_000017.11:73169178:C:G (self)
ss16737721, ss21433259 NT_010641.14:5057478:C:G NC_000017.11:73169178:C:G (self)
ss2286476, ss5694736, ss8819902, ss24214907, ss44036681, ss65748517, ss65941421, ss69201921, ss81496866, ss96609993, ss132637158, ss137176656, ss172523018, ss244279640 NT_010783.15:36439469:C:G NC_000017.11:73169178:C:G (self)
ss2952292734 NC_000017.10:71165317:C:T NC_000017.11:73169178:C:T (self)
13646875960 NC_000017.11:73169178:C:T NC_000017.11:73169178: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.

3 citations for rs1466113
PMID Title Author Year Journal
17903300 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. Fox CS et al. 2007 BMC medical genetics
20948194 The rs1466113 polymorphism in the somatostatin receptor 2 gene is associated with obesity and food intake in a Mediterranean population. Sotos-Prieto M et al. 2010 Annals of nutrition & metabolism
23828624 Association between polymorphisms in the P2RY1 and SSTR2 genes and sudden infant death syndrome. Läer K et al. 2013 International journal of legal medicine
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