Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs6449182 0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 27
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs806321 0.851 0.160 13 50267187 intron variant C/T snv 0.47 4