Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs863224451 0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214