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: rs104894966
rs104894966
SRY
3 0.882 0.200 Y 2787267 missense variant C/T snv 0.010 1.000 1 1993 1993
dbSNP: rs104894971
rs104894971
SRY
3 0.882 0.200 Y 2787551 missense variant C/T snv 4.4E-05 0.010 1.000 1 1998 1998
dbSNP: rs104894972
rs104894972
SRY
6 0.807 0.240 Y 2787320 missense variant C/T snv 0.010 1.000 1 2000 2000