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
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 27
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24