Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 1
rs1566734 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 1
rs35187787 0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 1
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 1
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 1
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 1
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 1
rs137853007 0.790 0.240 22 28725254 missense variant G/A;T snv 5.2E-05 2
rs121434507 0.925 0.080 11 48123636 missense variant C/T snv 4.0E-05 6.3E-05 1
rs119490107 0.925 0.080 8 94399540 missense variant C/A snv 2.8E-05 1
rs1339756947 1.000 0.080 17 21303189 missense variant C/A;T snv 2.0E-05 1
rs63750875 0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 1
rs28936407 0.925 0.080 3 12416831 missense variant G/A snv 8.0E-06 2.1E-05 1
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 1
rs587782705 0.807 0.280 17 7675157 missense variant G/A snv 8.0E-06 1
rs63751207 0.851 0.240 2 47466718 missense variant G/A;C;T snv 8.0E-06 1
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs63750781 0.851 0.160 3 37004444 missense variant C/G;T snv 4.0E-06 1
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs989026404 1.000 0.080 17 21304500 missense variant T/C;G snv 4.0E-06 1
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 5
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
rs121913341 0.851 0.280 7 140753350 missense variant A/C;T snv 2