Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555990470
rs1555990470
AR
A 0.700 GeneticVariation CLINVAR C601S mutation in the androgen receptor results in partial loss of androgen function. 20493947

2010
dbSNP: rs1555990470
rs1555990470
AR
A 0.700 GeneticVariation CLINVAR Two mutations causing complete androgen insensitivity: a frame-shift in the steroid binding domain and a Cys-->Phe substitution in the second zinc finger of the androgen receptor. 7981689

1994