Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 42
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs10680577 0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 19
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 55
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 26
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 28
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 30
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28