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rs1143699

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 2 In men, 2.19x risk of type 2 diabetes
Make rs1143699(C;T)
Make rs1143699(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position5210751
GenePTPRS
is asnp
is mentioned by
dbSNPrs1143699
dbSNP (old)rs1143699
ClinGenrs1143699
ebirs1143699
HLIrs1143699
Exacrs1143699
Varsomers1143699
Maprs1143699
PheGenIrs1143699
Biobankrs1143699
1000 genomesrs1143699
hgdprs1143699
ensemblrs1143699
gopubmedrs1143699
geneviewrs1143699
scholarrs1143699
googlers1143699
pharmgkbrs1143699
gwascentralrs1143699
openSNPrs1143699
23andMers1143699
23andMe allrs1143699
SNP Nexus

SNPshotrs1143699
SNPdbers1143699
MSV3drs1143699
GWAS Ctlgrs1143699
GMAF0.0932
Max Magnitude2
? (C;C) (C;T) (T;T) 28
[PMID 17893260] rs1143699, rs4807015, and rs1978237 confer an increased risk of developing type-2 diabetes "Logistic regression analysis demonstrated that for SNP rs1143699 in men, C/C homozygosity conveys an increased risk of T2D (OR = 2.19; P = 0.035)," (Abstract)
Neighborrs1978237
Distance1121