Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11779860
rs11779860
8 97838102 intron variant T/C snv 0.41
QT interval feature (observable entity)
0.700 1.000 1 2014 2014
dbSNP: rs2449539
rs2449539
1.000 0.160 8 97835027 intron variant T/C snv 7.1E-02
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2013 2013