AR, androgen receptor, 367

N. diseases: 854; N. variants: 163
Disease: Bulbo-Spinal Atrophy, X-Linked ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852573
rs137852573
Entrez Id: 367
Gene Symbol: AR
AR
CUI: C1839259
Disease:
Bulbo-Spinal Atrophy, X-Linked 		A 0.700 CausalMutation CLINVAR Male infertility and androgen receptor gene mutations: clinical features and identification of seven novel mutations. 17054461 2006
dbSNP: rs137852573
rs137852573
Entrez Id: 367
Gene Symbol: AR
AR
CUI: C1839259
Disease:
Bulbo-Spinal Atrophy, X-Linked 		A 0.700 CausalMutation CLINVAR Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene. 11788616 2002
dbSNP: rs137852573
rs137852573
Entrez Id: 367
Gene Symbol: AR
AR
CUI: C1839259
Disease:
Bulbo-Spinal Atrophy, X-Linked 		A 0.700 CausalMutation CLINVAR The clinical and molecular spectrum of androgen insensitivity syndromes. 8723113 1996
dbSNP: rs137852573
rs137852573
Entrez Id: 367
Gene Symbol: AR
AR
CUI: C1839259
Disease:
Bulbo-Spinal Atrophy, X-Linked 		A 0.700 CausalMutation CLINVAR Clinical and biochemical investigations and molecular analysis of subjects with mutations in the androgen receptor gene. 9039340 1996