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rs4502156

From SNPedia

Orientationplus
Stabilizedplus
Make rs4502156(C;C)
Make rs4502156(C;T)
Make rs4502156(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position62090956
is asnp
is mentioned by
dbSNPrs4502156
ebirs4502156
HLIrs4502156
Exacrs4502156
Varsomers4502156
Maprs4502156
PheGenIrs4502156
hapmaprs4502156
1000 genomesrs4502156
hgdprs4502156
ensemblrs4502156
gopubmedrs4502156
geneviewrs4502156
scholarrs4502156
googlers4502156
pharmgkbrs4502156
gwascentralrs4502156
openSNPrs4502156
23andMers4502156
23andMe allrs4502156
SNP Nexus

SNPshotrs4502156
SNPdbers4502156
MSV3drs4502156
GWAS Ctlgrs4502156
GMAF0.4431
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21873549OA-icon.png]
Trait
Title Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
Risk Allele T
P-val 4E-20
Odds Ratio None None