Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
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 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24