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: rs137852564
rs137852564
AR
5 0.827 0.240 X 67722976 missense variant G/A;T snv 0.700 0
dbSNP: rs137852574
rs137852574
AR
2 0.925 0.160 X 67723688 missense variant T/G snv 0.700 0
dbSNP: rs137852588
rs137852588
AR
2 0.925 0.160 X 67643284 missense variant C/T snv 0.700 0