Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Compensated hypothyroidism
CUI: C0342162
Disease: Compensated hypothyroidism
0.010 GeneticVariation BEFREE Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese. 17526952 2006