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rs7957197

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs7957197(A;A)
Make rs7957197(A;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position121022883
GeneOASL
is asnp
is mentioned by
dbSNPrs7957197
ebirs7957197
HLIrs7957197
Exacrs7957197
Varsomers7957197
Maprs7957197
PheGenIrs7957197
hapmaprs7957197
1000 genomesrs7957197
hgdprs7957197
ensemblrs7957197
gopubmedrs7957197
geneviewrs7957197
scholarrs7957197
googlers7957197
pharmgkbrs7957197
gwascentralrs7957197
openSNPrs7957197
23andMers7957197
23andMe allrs7957197
SNP Nexus

SNPshotrs7957197
SNPdbers7957197
MSV3drs7957197
GWAS Ctlgrs7957197
GMAF0.1313
Max Magnitude0
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 20581827OA-icon.png]
Trait Type 2 diabetes
Title Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Risk Allele T
P-val 2E-8
Odds Ratio 1.07 [1.05-1.10]


[PMID 21278902OA-icon.png] Genetic risk profiling for prediction of type 2 diabetes.


[PMID 22996131OA-icon.png] Monogenic models: what have the single gene disorders taught us?


[PMID 23462794OA-icon.png] Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets.