Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
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
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs764803020 0.851 0.040 17 7673750 frameshift variant -/TTTCCGCCGG delins 4.0E-06 5
rs781490101 0.851 0.040 17 7673748 missense variant T/C snv 8.0E-06 5
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs942158624 0.724 0.320 17 7674948 missense variant T/A snv 19
rs118101777 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs121913503 0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16