Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12101261
rs12101261
TSHR
0.810 GeneticVariation BEFREE These findings indicate that rs12101261 and rs179243 are the possible causal SNPs for GD susceptibility in the TSHR gene and could serve as genetic markers to predict the outcome of pTRAb+ in GD patients. 24144966

2014
dbSNP: rs12101261
rs12101261
TSHR
T 0.810 GeneticVariation GWASCAT A genome-wide association study identifies two new risk loci for Graves' disease. 21841780

2011
dbSNP: rs12101261
rs12101261
TSHR
T 0.810 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780

2011