Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2277923
rs2277923
NKX2-5
0.010 GeneticVariation BEFREE There was a significance association between 63A>G variation with primary hypothyroidism (p=0.003). 28749785

2017
dbSNP: rs763679435
rs763679435
TSHR ; LOC101928462
0.010 GeneticVariation BEFREE Congenital primary hypothyroidism in a turkish family caused by a homozygous nonsense mutation (R609X) in the thyrotropin receptor gene. 15671778

2004