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 213
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 37
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 37
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 19
rs778212685 0.827 0.120 22 28712015 missense variant C/A;G;T snv 4.0E-06 8