Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137852576
rs137852576
AR
5 0.827 0.240 X 67686067 missense variant G/A snv 0.030 1.000 3 1993 1999
dbSNP: rs137852573
rs137852573
AR
6 0.807 0.280 X 67686064 missense variant G/A snv 0.020 1.000 2 1997 1999
dbSNP: rs137852593
rs137852593
AR
8 0.827 0.160 X 67717484 missense variant G/A;C;T snv 2.2E-05; 1.1E-05; 9.1E-04 0.010 1.000 1 2003 2003