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: rs104894972
rs104894972
SRY
6 0.807 0.240 Y 2787320 missense variant C/T snv 0.010 1.000 1 2000 2000
dbSNP: rs1217301314
rs1217301314
5 0.827 0.240 11 57333494 missense variant T/C snv 1.2E-05 2.1E-05 0.010 1.000 1 2000 2000