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-06 484
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 221
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 181
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 56
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 42
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 37
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36