Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 16
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs1057519904 0.742 0.080 6 27872233 missense variant T/A snv 17
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs121913503 0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs149840192 0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs771563543 0.851 0.040 10 31510841 missense variant G/A snv 4.0E-06 1.4E-05 5
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs374052197 0.882 0.040 1 13610421 missense variant G/A;T snv 8.0E-06 5
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44