Source: ALL
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: 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