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.

rs9442372

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:1083324 (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
A>C / A>G / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.404802 (107147/264690, TOPMED)
A=0.419232 (91546/218366, ALFA)
A=0.421773 (59028/139952, GnomAD) (+ 19 more)
A=0.36017 (28142/78136, PAGE_STUDY)
A=0.18562 (3111/16760, 8.3KJPN)
A=0.3890 (1948/5008, 1000G)
A=0.4875 (2184/4480, Estonian)
A=0.4139 (1595/3854, ALSPAC)
A=0.4207 (1560/3708, TWINSUK)
A=0.2044 (599/2930, KOREAN)
A=0.3455 (720/2084, HGDP_Stanford)
A=0.4312 (809/1876, HapMap)
A=0.437 (436/998, GoNL)
A=0.178 (138/774, PRJEB37584)
A=0.475 (285/600, NorthernSweden)
A=0.236 (115/488, SGDP_PRJ)
G=0.486 (105/216, Qatari)
A=0.164 (35/214, Vietnamese)
A=0.38 (32/84, Ancient Sardinia)
A=0.38 (16/42, Siberian)
A=0.50 (20/40, GENOME_DK)
G=0.50 (20/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
C1orf159 : 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 1 NC_000001.11:g.1083324A>C
GRCh38.p13 chr 1 NC_000001.11:g.1083324A>G
GRCh38.p13 chr 1 NC_000001.11:g.1083324A>T
GRCh37.p13 chr 1 NC_000001.10:g.1018704A>C
GRCh37.p13 chr 1 NC_000001.10:g.1018704A>G
GRCh37.p13 chr 1 NC_000001.10:g.1018704A>T
Gene: C1orf159, chromosome 1 open reading frame 159 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
C1orf159 transcript variant 1 NM_001330306.2:c.1049-337…

NM_001330306.2:c.1049-337T>G

N/A Intron Variant
C1orf159 transcript variant 3 NM_001363525.2:c.941-337T…

NM_001363525.2:c.941-337T>G

N/A Intron Variant
C1orf159 transcript variant 2 NM_017891.5:c.503-337T>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

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 218366 A=0.419232 C=0.000000, G=0.580768
European Sub 191004 A=0.424279 C=0.000000, G=0.575721
African Sub 6820 A=0.4304 C=0.0000, G=0.5696
African Others Sub 228 A=0.461 C=0.000, G=0.539
African American Sub 6592 A=0.4293 C=0.0000, G=0.5707
Asian Sub 646 A=0.204 C=0.000, G=0.796
East Asian Sub 536 A=0.177 C=0.000, G=0.823
Other Asian Sub 110 A=0.336 C=0.000, G=0.664
Latin American 1 Sub 826 A=0.407 C=0.000, G=0.593
Latin American 2 Sub 7674 A=0.2871 C=0.0000, G=0.7129
South Asian Sub 5036 A=0.4623 C=0.0000, G=0.5377
Other Sub 6360 A=0.4046 C=0.0000, G=0.5954


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 A=0.404802 G=0.595198
Allele Frequency Aggregator Total Global 218366 A=0.419232 C=0.000000, G=0.580768
Allele Frequency Aggregator European Sub 191004 A=0.424279 C=0.000000, G=0.575721
Allele Frequency Aggregator Latin American 2 Sub 7674 A=0.2871 C=0.0000, G=0.7129
Allele Frequency Aggregator African Sub 6820 A=0.4304 C=0.0000, G=0.5696
Allele Frequency Aggregator Other Sub 6360 A=0.4046 C=0.0000, G=0.5954
Allele Frequency Aggregator South Asian Sub 5036 A=0.4623 C=0.0000, G=0.5377
Allele Frequency Aggregator Latin American 1 Sub 826 A=0.407 C=0.000, G=0.593
Allele Frequency Aggregator Asian Sub 646 A=0.204 C=0.000, G=0.796
gnomAD - Genomes Global Study-wide 139952 A=0.421773 G=0.578227
gnomAD - Genomes European Sub 75802 A=0.44852 G=0.55148
gnomAD - Genomes African Sub 41906 A=0.42323 G=0.57677
gnomAD - Genomes American Sub 13640 A=0.32229 G=0.67771
gnomAD - Genomes Ashkenazi Jewish Sub 3324 A=0.4037 G=0.5963
gnomAD - Genomes East Asian Sub 3128 A=0.2260 G=0.7740
gnomAD - Genomes Other Sub 2152 A=0.3941 G=0.6059
The PAGE Study Global Study-wide 78136 A=0.36017 G=0.63983
The PAGE Study AfricanAmerican Sub 32162 A=0.41832 G=0.58168
The PAGE Study Mexican Sub 10768 A=0.29309 G=0.70691
The PAGE Study Asian Sub 8294 A=0.2000 G=0.8000
The PAGE Study PuertoRican Sub 7882 A=0.3820 G=0.6180
The PAGE Study NativeHawaiian Sub 4502 A=0.3261 G=0.6739
The PAGE Study Cuban Sub 4204 A=0.4244 G=0.5756
The PAGE Study Dominican Sub 3812 A=0.3919 G=0.6081
The PAGE Study CentralAmerican Sub 2438 A=0.2945 G=0.7055
The PAGE Study SouthAmerican Sub 1974 A=0.2908 G=0.7092
The PAGE Study NativeAmerican Sub 1254 A=0.3724 G=0.6276
The PAGE Study SouthAsian Sub 846 A=0.422 G=0.578
8.3KJPN JAPANESE Study-wide 16760 A=0.18562 G=0.81438
1000Genomes Global Study-wide 5008 A=0.3890 G=0.6110
1000Genomes African Sub 1322 A=0.4902 G=0.5098
1000Genomes East Asian Sub 1008 A=0.2073 G=0.7927
1000Genomes Europe Sub 1006 A=0.4404 G=0.5596
1000Genomes South Asian Sub 978 A=0.438 G=0.562
1000Genomes American Sub 694 A=0.317 G=0.683
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.4875 G=0.5125
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.4139 G=0.5861
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.4207 G=0.5793
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.2044 G=0.7956, T=0.0000
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.3455 G=0.6545
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.194 G=0.806
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.413 G=0.587
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.494 G=0.506
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.428 G=0.572
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.426 G=0.574
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.148 G=0.852
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.18 G=0.82
HapMap Global Study-wide 1876 A=0.4312 G=0.5688
HapMap American Sub 766 A=0.379 G=0.621
HapMap African Sub 680 A=0.554 G=0.446
HapMap Asian Sub 254 A=0.217 G=0.783
HapMap Europe Sub 176 A=0.494 G=0.506
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.437 G=0.563
CNV burdens in cranial meningiomas Global Study-wide 774 A=0.178 G=0.822
CNV burdens in cranial meningiomas CRM Sub 774 A=0.178 G=0.822
Northern Sweden ACPOP Study-wide 600 A=0.475 G=0.525
SGDP_PRJ Global Study-wide 488 A=0.236 G=0.764
Qatari Global Study-wide 216 A=0.514 G=0.486
A Vietnamese Genetic Variation Database Global Study-wide 214 A=0.164 G=0.836
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 84 A=0.38 G=0.62
Siberian Global Study-wide 42 A=0.38 G=0.62
The Danish reference pan genome Danish Study-wide 40 A=0.50 G=0.50
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 A= C G T
GRCh38.p13 chr 1 NC_000001.11:g.1083324= NC_000001.11:g.1083324A>C NC_000001.11:g.1083324A>G NC_000001.11:g.1083324A>T
GRCh37.p13 chr 1 NC_000001.10:g.1018704= NC_000001.10:g.1018704A>C NC_000001.10:g.1018704A>G NC_000001.10:g.1018704A>T
C1orf159 transcript variant 1 NM_001330306.2:c.1049-337= NM_001330306.2:c.1049-337T>G NM_001330306.2:c.1049-337T>C NM_001330306.2:c.1049-337T>A
C1orf159 transcript variant 3 NM_001363525.2:c.941-337= NM_001363525.2:c.941-337T>G NM_001363525.2:c.941-337T>C NM_001363525.2:c.941-337T>A
C1orf159 transcript variant 2 NM_017891.4:c.503-337= NM_017891.4:c.503-337T>G NM_017891.4:c.503-337T>C NM_017891.4:c.503-337T>A
C1orf159 transcript variant 2 NM_017891.5:c.503-337= NM_017891.5:c.503-337T>G NM_017891.5:c.503-337T>C NM_017891.5:c.503-337T>A
C1orf159 transcript variant X1 XM_005244764.1:c.1049-337= XM_005244764.1:c.1049-337T>G XM_005244764.1:c.1049-337T>C XM_005244764.1:c.1049-337T>A
C1orf159 transcript variant X16 XM_005244765.1:c.941-337= XM_005244765.1:c.941-337T>G XM_005244765.1:c.941-337T>C XM_005244765.1:c.941-337T>A
C1orf159 transcript variant X3 XM_005244766.1:c.611-337= XM_005244766.1:c.611-337T>G XM_005244766.1:c.611-337T>C XM_005244766.1:c.611-337T>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#.

120 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_SNP ss13052166 Dec 05, 2003 (119)
2 CSHL-HAPMAP ss17377731 Feb 27, 2004 (120)
3 ABI ss41241520 Mar 14, 2006 (126)
4 ILLUMINA ss67918029 Dec 01, 2006 (127)
5 ILLUMINA ss68042957 Dec 01, 2006 (127)
6 ILLUMINA ss68303584 Dec 12, 2006 (127)
7 PERLEGEN ss68756311 May 18, 2007 (127)
8 ILLUMINA ss71607611 May 18, 2007 (127)
9 ILLUMINA ss75452698 Dec 07, 2007 (129)
10 AFFY ss76607731 Dec 08, 2007 (130)
11 HGSV ss83902725 Dec 15, 2007 (130)
12 KRIBB_YJKIM ss84819409 Dec 15, 2007 (130)
13 HGSV ss85972626 Dec 15, 2007 (130)
14 BCMHGSC_JDW ss87158097 Mar 23, 2008 (129)
15 ILLUMINA ss98259538 May 25, 2008 (130)
16 HUMANGENOME_JCVI ss99179684 Feb 05, 2009 (130)
17 BGI ss102713554 Dec 01, 2009 (131)
18 1000GENOMES ss107938554 Jan 22, 2009 (130)
19 1000GENOMES ss109940817 Jan 24, 2009 (130)
20 ENSEMBL ss137754350 Dec 01, 2009 (131)
21 ILLUMINA ss154494074 Dec 01, 2009 (131)
22 GMI ss154527283 Dec 01, 2009 (131)
23 ILLUMINA ss159668083 Dec 01, 2009 (131)
24 ILLUMINA ss160987366 Dec 01, 2009 (131)
25 COMPLETE_GENOMICS ss162982912 Jul 04, 2010 (132)
26 COMPLETE_GENOMICS ss163706949 Jul 04, 2010 (132)
27 COMPLETE_GENOMICS ss165982079 Jul 04, 2010 (132)
28 ILLUMINA ss174842643 Jul 04, 2010 (132)
29 BUSHMAN ss197888370 Jul 04, 2010 (132)
30 BCM-HGSC-SUB ss205215648 Jul 04, 2010 (132)
31 1000GENOMES ss218191728 Jul 14, 2010 (132)
32 1000GENOMES ss230396319 Jul 14, 2010 (132)
33 1000GENOMES ss238115882 Jul 15, 2010 (132)
34 BL ss252866235 May 09, 2011 (134)
35 GMI ss275682301 May 04, 2012 (137)
36 GMI ss283987994 Apr 25, 2013 (138)
37 PJP ss290494292 May 09, 2011 (134)
38 ILLUMINA ss481900328 May 04, 2012 (137)
39 ILLUMINA ss481933441 May 04, 2012 (137)
40 ILLUMINA ss482890570 Sep 08, 2015 (146)
41 ILLUMINA ss485744151 May 04, 2012 (137)
42 TISHKOFF ss553713109 Apr 25, 2013 (138)
43 SSMP ss647518190 Apr 25, 2013 (138)
44 ILLUMINA ss783317855 Sep 08, 2015 (146)
45 ILLUMINA ss832579399 Sep 08, 2015 (146)
46 ILLUMINA ss833178828 Jul 12, 2019 (153)
47 EVA-GONL ss974771686 Aug 21, 2014 (142)
48 JMKIDD_LAB ss1067613475 Aug 21, 2014 (142)
49 1000GENOMES ss1289348966 Aug 21, 2014 (142)
50 DDI ss1425685720 Apr 01, 2015 (144)
51 EVA_GENOME_DK ss1573851886 Apr 01, 2015 (144)
52 EVA_DECODE ss1584131583 Apr 01, 2015 (144)
53 EVA_UK10K_ALSPAC ss1599381903 Apr 01, 2015 (144)
54 EVA_UK10K_TWINSUK ss1642375936 Apr 01, 2015 (144)
55 EVA_SVP ss1712305536 Apr 01, 2015 (144)
56 ILLUMINA ss1751859839 Sep 08, 2015 (146)
57 HAMMER_LAB ss1793716480 Sep 08, 2015 (146)
58 WEILL_CORNELL_DGM ss1917963554 Feb 12, 2016 (147)
59 ILLUMINA ss1945981800 Feb 12, 2016 (147)
60 ILLUMINA ss1958230724 Feb 12, 2016 (147)
61 GENOMED ss1966667710 Jul 19, 2016 (147)
62 JJLAB ss2019499656 Sep 14, 2016 (149)
63 ILLUMINA ss2137493865 Nov 08, 2017 (151)
64 USC_VALOUEV ss2147486328 Dec 20, 2016 (150)
65 HUMAN_LONGEVITY ss2159383428 Dec 20, 2016 (150)
66 TOPMED ss2321522759 Dec 20, 2016 (150)
67 SYSTEMSBIOZJU ss2624265440 Nov 08, 2017 (151)
68 ILLUMINA ss2632465716 Nov 08, 2017 (151)
69 GRF ss2697377275 Nov 08, 2017 (151)
70 ILLUMINA ss2710663571 Nov 08, 2017 (151)
71 GNOMAD ss2750668067 Nov 08, 2017 (151)
72 AFFY ss2984841235 Nov 08, 2017 (151)
73 AFFY ss2985495004 Nov 08, 2017 (151)
74 SWEGEN ss2986153822 Nov 08, 2017 (151)
75 ILLUMINA ss3021043687 Nov 08, 2017 (151)
76 BIOINF_KMB_FNS_UNIBA ss3023514216 Nov 08, 2017 (151)
77 TOPMED ss3066463988 Nov 08, 2017 (151)
78 CSHL ss3343274059 Nov 08, 2017 (151)
79 ILLUMINA ss3625523506 Oct 11, 2018 (152)
80 ILLUMINA ss3633571474 Oct 11, 2018 (152)
81 ILLUMINA ss3634302054 Oct 11, 2018 (152)
82 ILLUMINA ss3635265678 Oct 11, 2018 (152)
83 ILLUMINA ss3635978704 Oct 11, 2018 (152)
84 ILLUMINA ss3637016018 Oct 11, 2018 (152)
85 ILLUMINA ss3637732488 Oct 11, 2018 (152)
86 ILLUMINA ss3638887862 Oct 11, 2018 (152)
87 ILLUMINA ss3639756837 Oct 11, 2018 (152)
88 ILLUMINA ss3640009420 Oct 11, 2018 (152)
89 ILLUMINA ss3640973166 Oct 11, 2018 (152)
90 ILLUMINA ss3641266981 Oct 11, 2018 (152)
91 ILLUMINA ss3642746763 Oct 11, 2018 (152)
92 ILLUMINA ss3643810768 Oct 11, 2018 (152)
93 ILLUMINA ss3644477663 Oct 11, 2018 (152)
94 URBANLAB ss3646581833 Oct 11, 2018 (152)
95 ILLUMINA ss3651365739 Oct 11, 2018 (152)
96 ILLUMINA ss3653614999 Oct 11, 2018 (152)
97 EGCUT_WGS ss3654264923 Jul 12, 2019 (153)
98 EVA_DECODE ss3685997303 Jul 12, 2019 (153)
99 ILLUMINA ss3724988430 Jul 12, 2019 (153)
100 ACPOP ss3726718425 Jul 12, 2019 (153)
101 ILLUMINA ss3744040776 Jul 12, 2019 (153)
102 ILLUMINA ss3744602985 Jul 12, 2019 (153)
103 EVA ss3745723896 Jul 12, 2019 (153)
104 PAGE_CC ss3770778807 Jul 12, 2019 (153)
105 ILLUMINA ss3772104743 Jul 12, 2019 (153)
106 PACBIO ss3783303002 Jul 12, 2019 (153)
107 PACBIO ss3788980790 Jul 12, 2019 (153)
108 PACBIO ss3793853339 Jul 12, 2019 (153)
109 KHV_HUMAN_GENOMES ss3798746536 Jul 12, 2019 (153)
110 EVA ss3825982473 Apr 25, 2020 (154)
111 EVA ss3836378996 Apr 25, 2020 (154)
112 EVA ss3841783023 Apr 25, 2020 (154)
113 HGDP ss3847322112 Apr 25, 2020 (154)
114 SGDP_PRJ ss3848003075 Apr 25, 2020 (154)
115 KRGDB ss3892845614 Apr 25, 2020 (154)
116 EVA ss3984450754 Apr 25, 2021 (155)
117 EVA ss3984774088 Apr 25, 2021 (155)
118 EVA ss4016889107 Apr 25, 2021 (155)
119 TOPMED ss4436510379 Apr 25, 2021 (155)
120 TOMMO_GENOMICS ss5142065330 Apr 25, 2021 (155)
121 1000Genomes NC_000001.10 - 1018704 Oct 11, 2018 (152)
122 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 1018704 Oct 11, 2018 (152)
123 Genetic variation in the Estonian population NC_000001.10 - 1018704 Oct 11, 2018 (152)
124 The Danish reference pan genome NC_000001.10 - 1018704 Apr 25, 2020 (154)
125 gnomAD - Genomes NC_000001.11 - 1083324 Apr 25, 2021 (155)
126 Genome of the Netherlands Release 5 NC_000001.10 - 1018704 Apr 25, 2020 (154)
127 HGDP-CEPH-db Supplement 1 NC_000001.9 - 1008567 Apr 25, 2020 (154)
128 HapMap NC_000001.11 - 1083324 Apr 25, 2020 (154)
129 KOREAN population from KRGDB NC_000001.10 - 1018704 Apr 25, 2020 (154)
130 Northern Sweden NC_000001.10 - 1018704 Jul 12, 2019 (153)
131 The PAGE Study NC_000001.11 - 1083324 Jul 12, 2019 (153)
132 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 1018704 Apr 25, 2021 (155)
133 CNV burdens in cranial meningiomas NC_000001.10 - 1018704 Apr 25, 2021 (155)
134 Qatari NC_000001.10 - 1018704 Apr 25, 2020 (154)
135 SGDP_PRJ NC_000001.10 - 1018704 Apr 25, 2020 (154)
136 Siberian NC_000001.10 - 1018704 Apr 25, 2020 (154)
137 8.3KJPN NC_000001.10 - 1018704 Apr 25, 2021 (155)
138 TopMed NC_000001.11 - 1083324 Apr 25, 2021 (155)
139 UK 10K study - Twins NC_000001.10 - 1018704 Oct 11, 2018 (152)
140 A Vietnamese Genetic Variation Database NC_000001.10 - 1018704 Jul 12, 2019 (153)
141 ALFA NC_000001.11 - 1083324 Apr 25, 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)
rs56444330 May 25, 2008 (130)
rs59721484 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
1177407575 NC_000001.11:1083323:A:C NC_000001.11:1083323:A:C
ss83902725, ss85972626, ss3638887862, ss3639756837, ss3643810768 NC_000001.8:1058626:A:G NC_000001.11:1083323:A:G (self)
4, ss76607731, ss87158097, ss107938554, ss109940817, ss162982912, ss163706949, ss165982079, ss197888370, ss205215648, ss252866235, ss275682301, ss283987994, ss290494292, ss481900328, ss1584131583, ss1712305536, ss2137493865, ss3642746763, ss3847322112 NC_000001.9:1008566:A:G NC_000001.11:1083323:A:G (self)
14055, 4248, 3171, 1359120, 2057, 23008, 3290, 15, 53, 5484, 20055, 2682, 34637, 4248, 977, ss218191728, ss230396319, ss238115882, ss481933441, ss482890570, ss485744151, ss553713109, ss647518190, ss783317855, ss832579399, ss833178828, ss974771686, ss1067613475, ss1289348966, ss1425685720, ss1573851886, ss1599381903, ss1642375936, ss1751859839, ss1793716480, ss1917963554, ss1945981800, ss1958230724, ss1966667710, ss2019499656, ss2147486328, ss2321522759, ss2624265440, ss2632465716, ss2697377275, ss2710663571, ss2750668067, ss2984841235, ss2985495004, ss2986153822, ss3021043687, ss3343274059, ss3625523506, ss3633571474, ss3634302054, ss3635265678, ss3635978704, ss3637016018, ss3637732488, ss3640009420, ss3640973166, ss3641266981, ss3644477663, ss3651365739, ss3653614999, ss3654264923, ss3726718425, ss3744040776, ss3744602985, ss3745723896, ss3772104743, ss3783303002, ss3788980790, ss3793853339, ss3825982473, ss3836378996, ss3848003075, ss3892845614, ss3984450754, ss3984774088, ss4016889107, ss5142065330 NC_000001.10:1018703:A:G NC_000001.11:1083323:A:G (self)
132943, 182, 276, 65212, 116714, 1177407575, ss2159383428, ss3023514216, ss3066463988, ss3646581833, ss3685997303, ss3724988430, ss3770778807, ss3798746536, ss3841783023, ss4436510379 NC_000001.11:1083323:A:G NC_000001.11:1083323:A:G (self)
ss41241520, ss67918029, ss68042957, ss68303584, ss68756311, ss71607611, ss75452698, ss84819409, ss98259538, ss99179684, ss102713554, ss137754350, ss154494074, ss154527283, ss159668083, ss160987366, ss174842643 NT_004350.19:497335:A:G NC_000001.11:1083323:A:G (self)
ss17377731 NT_077913.2:22414:A:G NC_000001.11:1083323:A:G (self)
ss13052166 NT_077960.1:90189:A:G NC_000001.11:1083323:A:G (self)
23008, ss3892845614 NC_000001.10:1018703:A:T NC_000001.11:1083323:A: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 rs9442372

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