Source: BEFREE ×
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: rs104894874
rs104894874
1 0.882 0.160 X 43958521 missense variant T/C snv 5.5E-06 0.010 1.000 1 2006 2006
dbSNP: rs28933684
rs28933684
2 0.882 0.160 X 43949831 missense variant G/A;T snv 0.010 1.000 1 1993 1993
dbSNP: rs774200714
rs774200714
1 1.000 0.160 11 86954909 missense variant G/T snv 3.6E-05 5.6E-05 0.010 1.000 1 1997 1997