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rs12101261

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs12101261
ClinGenrs12101261
ebirs12101261
HLIrs12101261
Exacrs12101261
Gnomadrs12101261
Varsomers12101261
LitVarrs12101261
Maprs12101261
PheGenIrs12101261
Biobankrs12101261
1000 genomesrs12101261
hgdprs12101261
ensemblrs12101261
geneviewrs12101261
scholarrs12101261
googlers12101261
pharmgkbrs12101261
gwascentralrs12101261
openSNPrs12101261
23andMers12101261
SNPshotrs12101261
SNPdbers12101261
MSV3drs12101261
GWAS Ctlgrs12101261
GMAF0.4449
Max Magnitude0
? (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]