Rs12101261

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Orientationplus
Make rs12101261(C;C)
Make rs12101261(C;T)
Make rs12101261(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position80984885
GeneTSHR
is asnp
is mentioned by
dbSNPrs12101261
Exacrs12101261
PheGenIrs12101261
nextbiors12101261
hapmaprs12101261
1000 genomesrs12101261
hgdprs12101261
ensemblrs12101261
gopubmedrs12101261
geneviewrs12101261
scholarrs12101261
googlers12101261
pharmgkbrs12101261
gwascentralrs12101261
openSNPrs12101261
23andMers12101261
23andMe allrs12101261
SNP Nexus

SNPshotrs12101261
SNPdbers12101261
MSV3drs12101261
GMAF0.4449
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21841780]
Trait
Title A genome-wide association study identifies two new risk loci for Graves' disease.
Risk Allele T
P-val 7E-24
Odds Ratio 1.3500 [1.28-1.43]