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: rs104894884
rs104894884
2 0.821 0.107 X 119871933 missense variant G/C snp 0.700 1 2007 2007
dbSNP: rs104894885
rs104894885
2 0.801 0.143 X 119873312 missense variant G/A,C snp 0.700 1 2007 2007