Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852569
rs137852569
AR
A 0.700 CausalMutation CLINVAR Clinical and molecular characteristics in 15 patients with androgen receptor gene mutations from South China. 28261839

2017
dbSNP: rs137852569
rs137852569
AR
A 0.700 CausalMutation CLINVAR Androgen insensitivity syndrome in a cohort of Sri Lankan children with 46, XY disorders of sex development (46, XY DSD). 26778393

2015
dbSNP: rs137852569
rs137852569
AR
A 0.700 CausalMutation CLINVAR Point mutation in the DNA binding domain of the androgen receptor in two families with Reifenstein syndrome. 1598912

1992