THRA, thyroid hormone receptor alpha, 7067

N. diseases: 124; N. variants: 12
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853162
rs137853162
Entrez Id: 7067
Gene Symbol: THRA
THRA
CUI: C3280817
Disease:
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6 		T 0.700 CausalMutation CLINVAR