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rs10842994

From SNPedia

Orientationplus
Stabilizedplus
Make rs10842994(C;C)
Make rs10842994(C;T)
Make rs10842994(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position27812217
is asnp
is mentioned by
dbSNPrs10842994
ebirs10842994
HLIrs10842994
Exacrs10842994
Varsomers10842994
Maprs10842994
PheGenIrs10842994
hapmaprs10842994
1000 genomesrs10842994
hgdprs10842994
ensemblrs10842994
gopubmedrs10842994
geneviewrs10842994
scholarrs10842994
googlers10842994
pharmgkbrs10842994
gwascentralrs10842994
openSNPrs10842994
23andMers10842994
23andMe allrs10842994
SNP Nexus

SNPshotrs10842994
SNPdbers10842994
MSV3drs10842994
GWAS Ctlgrs10842994
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 8E-6
Odds Ratio 1.09 [1.04-1.13]


[PMID 25951451OA-icon.png] Replication Study in a Japanese Population to Evaluate the Association between 10 SNP Loci, Identified in European Genome-Wide Association Studies, and Type 2 Diabetes