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rs10190052

From SNPedia

Orientationplus
Stabilizedplus
Make rs10190052(C;C)
Make rs10190052(C;T)
Make rs10190052(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position646674
is asnp
is mentioned by
dbSNPrs10190052
ebirs10190052
HLIrs10190052
Exacrs10190052
Varsomers10190052
Maprs10190052
PheGenIrs10190052
hapmaprs10190052
1000 genomesrs10190052
hgdprs10190052
ensemblrs10190052
gopubmedrs10190052
geneviewrs10190052
scholarrs10190052
googlers10190052
pharmgkbrs10190052
gwascentralrs10190052
openSNPrs10190052
23andMers10190052
23andMe allrs10190052
SNP Nexus

SNPshotrs10190052
SNPdbers10190052
MSV3drs10190052
GWAS Ctlgrs10190052
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24509480OA-icon.png]
Trait Type 2 diabetes
Title Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Risk Allele C
P-val 2E-7
Odds Ratio 1.07 [1.04-1.10]