Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555997580
rs1555997580
AR
T 0.700 CausalMutation CLINVAR Targeted next-generation sequencing identification of mutations in patients with disorders of sex development. 26980296

2016
dbSNP: rs1555997580
rs1555997580
AR
T 0.700 CausalMutation CLINVAR Androgen resistance due to mutation of the androgen receptor. 1458719

1992