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
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
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
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 83
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 26
rs121913444 0.724 0.160 7 55191831 missense variant T/A;C;G snv 17
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 16
rs1057519904 0.742 0.080 6 27872233 missense variant T/A snv 14
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 13
rs1553260624 0.763 0.080 1 226064454 missense variant G/A snv 13