Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14
rs74315452 0.732 0.160 21 31667356 missense variant T/C snv 12
rs80356726 0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs387906709 0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs387906711 0.807 0.120 X 56565389 missense variant C/A;T snv 6.6E-06 6