Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24