Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1163944538 0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1352010373 0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs1563183492 0.708 0.520 7 70766248 missense variant C/T snv 32
rs1554208945 0.752 0.240 6 87260207 missense variant A/C snv 26
rs1563686762 0.790 0.280 8 116847620 inframe deletion GTT/- delins 16
rs387906702 0.807 0.200 X 53403635 missense variant A/G snv 16
rs1567941252 0.807 0.240 17 38739601 missense variant G/A snv 10
rs1057519565 0.851 0.200 11 687941 missense variant C/T snv 9