Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1564421528
rs1564421528
WAC
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		T 0.700 CausalMutation CLINVAR

dbSNP: rs770374710
rs770374710
MAGEL2
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		TG 0.700 CausalMutation CLINVAR