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: rs764249635
rs764249635
SRY
1 1.000 0.160 Y 2787425 missense variant A/G snv 1.5E-05 0.700 1.000 20 1990 2007
dbSNP: rs104894973
rs104894973
SRY
1 1.000 0.160 Y 2787224 missense variant T/A;C snv 0.800 1.000 24 1990 2017