Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs121913341 0.851 0.280 7 140753350 missense variant A/C;T snv 2
rs137853007 0.790 0.240 22 28725254 missense variant G/A;T snv 5.2E-05 2
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 2
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs35187787 0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 1
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 1
rs63751012 0.851 0.200 3 36993656 stop gained G/A;C;T snv 1
rs119490107 0.925 0.080 8 94399540 missense variant C/A snv 2.8E-05 1
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 1
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 1
rs1339756947 1.000 0.080 17 21303189 missense variant C/A;T snv 2.0E-05 1
rs989026404 1.000 0.080 17 21304500 missense variant T/C;G snv 4.0E-06 1
rs587779021 0.851 0.200 3 37008905 missense variant G/A;C snv 1
rs63750206 0.807 0.200 3 36996701 missense variant G/A;C;T snv 1
rs63750781 0.851 0.160 3 37004444 missense variant C/G;T snv 4.0E-06 1
rs63750875 0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 1
rs63751207 0.851 0.240 2 47466718 missense variant G/A;C;T snv 8.0E-06 1
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 1
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 1
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 1