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 22
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 1
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 13
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 19
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 1
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 9
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 37
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 1