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dbSNP Short Genetic Variations

Reference SNP (rs) Report

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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.

rs592229

Current Build 151

Released July 17, 2018

Organism
Homo sapiens
Position
chr6:31962664 (GRCh38.p7) 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=0.39107 (94537/241740, GnomAD)
G=0.38679 (48568/125568, TOPMED)
G=0.3931 (12090/30758, GnomAD) (+ 4 more)
G=0.383 (3234/8440, GO-ESP)
G=0.348 (1742/5008, 1000G)
G=0.474 (1826/3854, ALSPAC)
G=0.485 (1798/3708, TWINSUK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SKIV2L : Intron Variant
Publications
3 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.p7 chr 6 NC_000006.12:g.31962664G>A
GRCh38.p7 chr 6 NC_000006.12:g.31962664G>C
GRCh38.p7 chr 6 NC_000006.12:g.31962664G>T
GRCh37.p13 chr 6 NC_000006.11:g.31930441G>A
GRCh37.p13 chr 6 NC_000006.11:g.31930441G>C
GRCh37.p13 chr 6 NC_000006.11:g.31930441G>T
SKIV2L RefSeqGene NG_032652.1:g.8861G>A
SKIV2L RefSeqGene NG_032652.1:g.8861G>C
SKIV2L RefSeqGene NG_032652.1:g.8861G>T
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.3440091G>A
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.3440091G>C
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.3440091G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.3440197G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.3440197G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.3440197G>T
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.3263853T>G
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.3263853T>A
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.3263853T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.3263151T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.3263151T>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.3263151T>C
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3304700T>G
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3304700T>A
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3304700T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3310285T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3310285T>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3310285T>C
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3218634T>G
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3218634T>A
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3218634T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3224230T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3224230T>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3224230T>C
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3210439T>G
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3210439T>A
GRCh38.p7 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3210439T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3216024T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3216024T>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3216024T>C
Gene: SKIV2L, Ski2 like RNA helicase (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SKIV2L transcript NM_006929.4:c. N/A Intron Variant
SKIV2L transcript variant X1 XM_011514815.2:c. N/A Intron Variant
SKIV2L transcript variant X2 XR_001743586.1:n. N/A Intron Variant
SKIV2L transcript variant X3 XR_926301.2: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
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
Trans-Omics for Precision Medicine Global Study-wide 125568 G=0.38679 T=0.61321
The Genome Aggregation Database Global Study-wide 30758 G=0.3931 T=0.6069
The Genome Aggregation Database European Sub 18386 G=0.4325 T=0.5675
The Genome Aggregation Database African Sub 8664 G=0.309 T=0.691
The Genome Aggregation Database East Asian Sub 1604 G=0.423 T=0.577
The Genome Aggregation Database Other Sub 976 G=0.41 T=0.59
The Genome Aggregation Database American Sub 834 G=0.37 T=0.63
The Genome Aggregation Database Ashkenazi Jewish Sub 294 G=0.22 T=0.78
GO Exome Sequencing Project Global Study-wide 8440 G=0.383 T=0.617
GO Exome Sequencing Project European American Sub 5418 G=0.436 T=0.564
GO Exome Sequencing Project African American Sub 3022 G=0.289 T=0.711
1000Genomes Global Study-wide 5008 G=0.348 T=0.652
1000Genomes African Sub 1322 G=0.235 T=0.765
1000Genomes East Asian Sub 1008 G=0.458 T=0.542
1000Genomes Europe Sub 1006 G=0.373 T=0.627
1000Genomes South Asian Sub 978 G=0.33 T=0.67
1000Genomes American Sub 694 G=0.39 T=0.61
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.474 T=0.526
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.485 T=0.515
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 Note
GRCh38.p7 chr 6 NC_000006.12:...

NC_000006.12:g.31962664G=

NC_000006.12:...

NC_000006.12:g.31962664G>A

NC_000006.12:...

NC_000006.12:g.31962664G>C

NC_000006.12:...

NC_000006.12:g.31962664G>T

GRCh37.p13 chr 6 NC_000006.11:...

NC_000006.11:g.31930441G=

NC_000006.11:...

NC_000006.11:g.31930441G>A

NC_000006.11:...

NC_000006.11:g.31930441G>C

NC_000006.11:...

NC_000006.11:g.31930441G>T

SKIV2L RefSeqGene NG_032652.1:g...

NG_032652.1:g.8861G=

NG_032652.1:g...

NG_032652.1:g.8861G>A

NG_032652.1:g...

NG_032652.1:g.8861G>C

NG_032652.1:g...

NG_032652.1:g.8861G>T

GRCh38.p7 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g...

NT_113891.3:g.3440091G=

NT_113891.3:g...

NT_113891.3:g.3440091G>A

NT_113891.3:g...

NT_113891.3:g.3440091G>C

NT_113891.3:g...

NT_113891.3:g.3440091G>T

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g...

NT_113891.2:g.3440197G=

NT_113891.2:g...

NT_113891.2:g.3440197G>A

NT_113891.2:g...

NT_113891.2:g.3440197G>C

NT_113891.2:g...

NT_113891.2:g.3440197G>T

GRCh38.p7 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g...

NT_167249.2:g.3263853T>G

NT_167249.2:g...

NT_167249.2:g.3263853T>A

NT_167249.2:g...

NT_167249.2:g.3263853T>C

NT_167249.2:g...

NT_167249.2:g.3263853T=

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g...

NT_167249.1:g.3263151T>G

NT_167249.1:g...

NT_167249.1:g.3263151T>A

NT_167249.1:g...

NT_167249.1:g.3263151T>C

NT_167249.1:g...

NT_167249.1:g.3263151T=

GRCh38.p7 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g...

NT_167247.2:g.3304700T>G

NT_167247.2:g...

NT_167247.2:g.3304700T>A

NT_167247.2:g...

NT_167247.2:g.3304700T>C

NT_167247.2:g...

NT_167247.2:g.3304700T=

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g...

NT_167247.1:g.3310285T>G

NT_167247.1:g...

NT_167247.1:g.3310285T>A

NT_167247.1:g...

NT_167247.1:g.3310285T>C

NT_167247.1:g...

NT_167247.1:g.3310285T=

GRCh38.p7 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g...

NT_167248.2:g.3218634T>G

NT_167248.2:g...

NT_167248.2:g.3218634T>A

NT_167248.2:g...

NT_167248.2:g.3218634T>C

NT_167248.2:g...

NT_167248.2:g.3218634T=

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g...

NT_167248.1:g.3224230T>G

NT_167248.1:g...

NT_167248.1:g.3224230T>A

NT_167248.1:g...

NT_167248.1:g.3224230T>C

NT_167248.1:g...

NT_167248.1:g.3224230T=

GRCh38.p7 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g...

NT_167245.2:g.3210439T>G

NT_167245.2:g...

NT_167245.2:g.3210439T>A

NT_167245.2:g...

NT_167245.2:g.3210439T>C

NT_167245.2:g...

NT_167245.2:g.3210439T=

GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g...

NT_167245.1:g.3216024T>G

NT_167245.1:g...

NT_167245.1:g.3216024T>A

NT_167245.1:g...

NT_167245.1:g.3216024T>C

NT_167245.1:g...

NT_167245.1:g.3216024T=

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#.

7 Frequency, 106 SubSNP submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss764014 Aug 11, 2000 (83)
2 TSC-CSHL ss1342990 Oct 08, 2002 (110)
3 KWOK ss1955545 Oct 18, 2000 (87)
4 SC_JCM ss2580896 Nov 09, 2000 (92)
5 YUSUKE ss2990671 Jun 15, 2001 (96)
6 HGBASE ss3184388 Aug 15, 2001 (98)
7 TSC-CSHL ss5248646 Oct 08, 2002 (110)
8 WI_SSAHASNP ss11827871 Jul 11, 2003 (117)
9 SI_MHC_SNP ss12692014 Oct 31, 2003 (118)
10 CSHL-HAPMAP ss17887351 Feb 27, 2004 (120)
11 SSAHASNP ss22486887 Apr 05, 2004 (121)
12 PERLEGEN ss24362129 Sep 20, 2004 (123)
13 ABI ss44723481 Mar 13, 2006 (126)
14 ILLUMINA ss65760909 Oct 16, 2006 (127)
15 ILLUMINA ss66545552 Dec 02, 2006 (127)
16 ILLUMINA ss67425614 Dec 02, 2006 (127)
17 ILLUMINA ss67784397 Dec 02, 2006 (127)
18 PERLEGEN ss68971818 May 18, 2007 (127)
19 ILLUMINA ss70849710 May 24, 2008 (130)
20 ILLUMINA ss71434834 May 18, 2007 (127)
21 ILLUMINA ss75675912 Dec 07, 2007 (129)
22 ILLUMINA ss79211381 Dec 14, 2007 (130)
23 HGSV ss85373337 Dec 14, 2007 (130)
24 HUMANGENOME_JCVI ss98379987 Feb 04, 2009 (130)
25 BGI ss104297021 Dec 01, 2009 (131)
26 1000GENOMES ss109902840 Feb 13, 2009 (136)
27 1000GENOMES ss114147276 Jan 25, 2009 (136)
28 ILLUMINA-UK ss116395604 Feb 14, 2009 (130)
29 ILLUMINA ss122483974 Dec 01, 2009 (131)
30 ENSEMBL ss139561036 Dec 01, 2009 (131)
31 ILLUMINA ss154343865 Dec 01, 2009 (131)
32 ILLUMINA ss159520395 Dec 01, 2009 (131)
33 ILLUMINA ss160750034 Dec 01, 2009 (131)
34 COMPLETE_GENOMICS ss162199940 Jul 04, 2010 (132)
35 COMPLETE_GENOMICS ss163350338 Jul 04, 2010 (132)
36 COMPLETE_GENOMICS ss166431597 Jul 04, 2010 (132)
37 ILLUMINA ss172056407 Jul 04, 2010 (132)
38 ILLUMINA ss173939889 Jul 04, 2010 (132)
39 BUSHMAN ss201628441 Jul 04, 2010 (132)
40 BCM-HGSC-SUB ss207561504 Jul 04, 2010 (132)
41 1000GENOMES ss222305023 Jul 14, 2010 (136)
42 1000GENOMES ss233400021 Jul 14, 2010 (136)
43 1000GENOMES ss240470578 Jul 15, 2010 (136)
44 BL ss254188889 May 09, 2011 (136)
45 GMI ss278728005 May 04, 2012 (137)
46 PJP ss293826337 May 09, 2011 (136)
47 ILLUMINA ss410939352 Sep 17, 2011 (136)
48 ILLUMINA ss482179944 Sep 08, 2015 (146)
49 EXOME_CHIP ss491382485 May 04, 2012 (137)
50 ILLUMINA ss537319741 Sep 08, 2015 (146)
51 TISHKOFF ss559115509 Apr 25, 2013 (138)
52 SSMP ss653037290 Apr 25, 2013 (138)
53 NHLBI-ESP ss712700661 Apr 25, 2013 (138)
54 ILLUMINA ss778707579 Sep 08, 2015 (146)
55 ILLUMINA ss780685671 Sep 08, 2015 (146)
56 ILLUMINA ss783359167 Sep 08, 2015 (146)
57 ILLUMINA ss825541899 Apr 01, 2015 (144)
58 ILLUMINA ss834166680 Sep 08, 2015 (146)
59 EVA-GONL ss982769170 Aug 21, 2014 (142)
60 1000GENOMES ss1319568234 Aug 21, 2014 (142)
61 EVA_GENOME_DK ss1581607876 Apr 01, 2015 (144)
62 EVA_UK10K_ALSPAC ss1615283010 Apr 01, 2015 (144)
63 EVA_UK10K_TWINSUK ss1658277043 Apr 01, 2015 (144)
64 EVA_EXAC ss1688245228 Apr 01, 2015 (144)
65 EVA_EXAC ss1688245229 Apr 01, 2015 (144)
66 EVA_EXAC ss1688245230 Apr 01, 2015 (144)
67 EVA_MGP ss1711121953 Apr 01, 2015 (144)
68 EVA_SVP ss1712851486 Apr 01, 2015 (144)
69 ILLUMINA ss1752629715 Sep 08, 2015 (146)
70 HAMMER_LAB ss1804359140 Sep 08, 2015 (146)
71 ILLUMINA ss1917802952 Feb 12, 2016 (147)
72 WEILL_CORNELL_DGM ss1926021253 Feb 12, 2016 (147)
73 ILLUMINA ss1946173956 Feb 12, 2016 (147)
74 ILLUMINA ss1958889657 Feb 12, 2016 (147)
75 GENOMED ss1970358016 Jul 19, 2016 (147)
76 JJLAB ss2023643956 Sep 14, 2016 (149)
77 ILLUMINA ss2094825182 Dec 20, 2016 (150)
78 ILLUMINA ss2095178437 Dec 20, 2016 (150)
79 USC_VALOUEV ss2151810830 Dec 20, 2016 (150)
80 HUMAN_LONGEVITY ss2282965640 Dec 20, 2016 (150)
81 TOPMED ss2451341252 Dec 20, 2016 (150)
82 SYSTEMSBIOZJU ss2626309379 Nov 08, 2017 (151)
83 ILLUMINA ss2634430937 Nov 08, 2017 (151)
84 ILLUMINA ss2635155758 Nov 08, 2017 (151)
85 GRF ss2707404551 Nov 08, 2017 (151)
86 GNOMAD ss2735671376 Nov 08, 2017 (151)
87 GNOMAD ss2747588063 Nov 08, 2017 (151)
88 GNOMAD ss2837457639 Nov 08, 2017 (151)
89 AFFY ss2985362958 Nov 08, 2017 (151)
90 AFFY ss2985994891 Nov 08, 2017 (151)
91 SWEGEN ss2998801152 Nov 08, 2017 (151)
92 ILLUMINA ss3022600755 Nov 08, 2017 (151)
93 BIOINF_KMB_FNS_UNIBA ss3025608942 Nov 08, 2017 (151)
94 TOPMED ss3493913469 Nov 08, 2017 (151)
95 ILLUMINA ss3625898204 Jul 20, 2018 (151)
96 ILLUMINA ss3629505769 Jul 20, 2018 (151)
97 ILLUMINA ss3629505770 Jul 20, 2018 (151)
98 ILLUMINA ss3632349337 Jul 20, 2018 (151)
99 ILLUMINA ss3635058052 Jul 20, 2018 (151)
100 ILLUMINA ss3636779066 Jul 20, 2018 (151)
101 ILLUMINA ss3638620623 Jul 20, 2018 (151)
102 ILLUMINA ss3639311634 Jul 20, 2018 (151)
103 ILLUMINA ss3639681278 Jul 20, 2018 (151)
104 ILLUMINA ss3640765351 Jul 20, 2018 (151)
105 ILLUMINA ss3643562040 Jul 20, 2018 (151)
106 ILLUMINA ss3644907029 Jul 20, 2018 (151)
107 1000Genomes NC_000006.11 - 31930441 Jul 20, 2018 (151)
108 The Avon Longitudinal Study of Parents and Children NC_000006.11 - 31930441 Jul 20, 2018 (151)
109 The Genome Aggregation Database NC_000006.11 - 31930441 Jul 20, 2018 (151)
110 The Genome Aggregation Database NC_000006.11 - 31930441 Jul 20, 2018 (151)
111 GO Exome Sequencing Project NC_000006.11 - 31930441 Jul 20, 2018 (151)
112 Trans-Omics for Precision Medicine NC_000006.12 - 31962664 Jul 20, 2018 (151)
113 UK 10K study - Twins NC_000006.11 - 31930441 Jul 20, 2018 (151)
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)
rs909162 Oct 23, 2000 (87)
rs1738437 Jan 18, 2001 (92)
rs3880458 Dec 16, 2002 (110)
rs7768734 Aug 27, 2003 (117)
rs17566427 Oct 08, 2004 (123)
rs57814915 May 24, 2008 (130)
rs114592706 Mar 28, 2012 (136)
rs117140783 Aug 16, 2010 (132)
Added to this RefSNP Cluster:
Submission ids Observation SPDI Canonical SPDI Source RSIDs
ss85373337, ss3639311634, ss3639681278 NC_000006.9:32038419:G= NC_000006.12:31962663:G= (self)
ss109902840, ss114147276, ss116395604, ss162199940, ss163350338, ss166431597, ss201628441, ss207561504, ss254188889, ss278728005, ss293826337, ss825541899, ss1712851486, ss2635155758, ss3643562040 NC_000006.10:32038419:G= NC_000006.12:31962663:G= (self)
31336080, 17473159, 178085396, 4686111, 630827, 17473159, ss222305023, ss233400021, ss240470578, ss482179944, ss491382485, ss537319741, ss559115509, ss653037290, ss712700661, ss778707579, ss780685671, ss783359167, ss834166680, ss982769170, ss1319568234, ss1581607876, ss1615283010, ss1658277043, ss1688245228, ss1688245229, ss1688245230, ss1711121953, ss1752629715, ss1804359140, ss1917802952, ss1926021253, ss1946173956, ss1958889657, ss1970358016, ss2023643956, ss2094825182, ss2095178437, ss2151810830, ss2451341252, ss2626309379, ss2634430937, ss2707404551, ss2735671376, ss2747588063, ss2837457639, ss2985362958, ss2985994891, ss2998801152, ss3022600755, ss3625898204, ss3629505769, ss3629505770, ss3632349337, ss3635058052, ss3636779066, ss3638620623, ss3640765351, ss3644907029 NC_000006.11:31930440:G= NC_000006.12:31962663:G= (self)
335097264, ss2282965640, ss3025608942, ss3493913469 NC_000006.12:31962663:G= NC_000006.12:31962663:G= (self)
ss11827871, ss17887351, ss22486887 NT_007592.13:22784906:G= NC_000006.12:31962663:G= (self)
ss764014, ss1342990, ss1955545, ss2580896, ss2990671, ss3184388, ss5248646, ss12692014, ss24362129, ss44723481, ss65760909, ss66545552, ss67425614, ss67784397, ss68971818, ss70849710, ss71434834, ss75675912, ss79211381, ss98379987, ss104297021, ss122483974, ss139561036, ss154343865, ss159520395, ss160750034, ss172056407, ss173939889, ss410939352 NT_007592.15:31870440:G= NC_000006.12:31962663:G= (self)
4686111, ss1688245230, ss2735671376 NC_000006.11:31930440:G>A NC_000006.12:31962663:G>A (self)
4686111, ss1688245229, ss2735671376 NC_000006.11:31930440:G>C NC_000006.12:31962663:G>C (self)
ss85373337, ss3639311634, ss3639681278 NC_000006.9:32038419:G>T NC_000006.12:31962663:G>T (self)
ss109902840, ss114147276, ss116395604, ss162199940, ss163350338, ss166431597, ss201628441, ss207561504, ss254188889, ss278728005, ss293826337, ss825541899, ss1712851486, ss2635155758, ss3643562040 NC_000006.10:32038419:G>T NC_000006.12:31962663:G>T (self)
31336080, 17473159, 178085396, 4686111, 630827, 17473159, ss222305023, ss233400021, ss240470578, ss482179944, ss491382485, ss537319741, ss559115509, ss653037290, ss712700661, ss778707579, ss780685671, ss783359167, ss834166680, ss982769170, ss1319568234, ss1581607876, ss1615283010, ss1658277043, ss1688245228, ss1711121953, ss1752629715, ss1804359140, ss1917802952, ss1926021253, ss1946173956, ss1958889657, ss1970358016, ss2023643956, ss2094825182, ss2095178437, ss2151810830, ss2451341252, ss2626309379, ss2634430937, ss2707404551, ss2735671376, ss2747588063, ss2837457639, ss2985362958, ss2985994891, ss2998801152, ss3022600755, ss3625898204, ss3629505769, ss3629505770, ss3632349337, ss3635058052, ss3636779066, ss3638620623, ss3640765351, ss3644907029 NC_000006.11:31930440:G>T NC_000006.12:31962663:G>T (self)
335097264, ss2282965640, ss3025608942, ss3493913469 NC_000006.12:31962663:G>T NC_000006.12:31962663:G>T (self)
ss11827871, ss17887351, ss22486887 NT_007592.13:22784906:G>T NC_000006.12:31962663:G>T (self)
ss764014, ss1342990, ss1955545, ss2580896, ss2990671, ss3184388, ss5248646, ss12692014, ss24362129, ss44723481, ss65760909, ss66545552, ss67425614, ss67784397, ss68971818, ss70849710, ss71434834, ss75675912, ss79211381, ss98379987, ss104297021, ss122483974, ss139561036, ss154343865, ss159520395, ss160750034, ss172056407, ss173939889, ss410939352 NT_007592.15:31870440:G>T NC_000006.12:31962663: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.

3 citations for rs592229
PMID Title Author Year Journal
23168575 Candidate gene linkage approach to identify DNA variants that predispose to preterm birth. Bream EN et al. 2013 Pediatric research
23889843 Gene expression changes with age in skin, adipose tissue, blood and brain. Glass D et al. 2013 Genome biology
24194833 Using information interaction to discover epistatic effects in complex diseases. Anunciação O et al. 2013 PloS one

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: 0.1.4.post833+d3ba21e