Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554888939 0.683 0.640 9 137798823 missense variant G/T snv 58
rs1553621496 0.677 0.440 2 209976305 splice donor variant T/G snv 53
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs1569509136 0.708 0.400 X 53647576 splice acceptor variant T/C snv 24