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: rs104894914
rs104894914
4 0.851 0.120 X 154191716 missense variant T/C snv 0.800 1.000 2 1992 2002
dbSNP: rs104894915
rs104894915
1 1.000 0.120 X 154187939 missense variant C/A snv 0.800 1.000 2 1992 2002
dbSNP: rs104894916
rs104894916
1 1.000 0.120 X 154195934 missense variant G/A snv 0.800 1.000 2 1992 2002
dbSNP: rs724159983
rs724159983
1 1.000 0.120 X 154182566 upstream gene variant A/C snv 0.700 0