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
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs750893877 0.807 0.320 17 7674258 synonymous variant G/A snv 8.0E-06 7
rs751306825
ALK
0.925 0.080 2 29220759 missense variant G/A;T snv 4.0E-06 4
rs73070954 0.925 0.040 2 208248572 missense variant C/T snv 3.5E-03 1.4E-02 2
rs749395621 0.925 0.040 15 90087536 missense variant T/C;G snv 4.0E-06; 3.6E-05 2
rs1244270149
ALK
1.000 0.040 2 29220746 missense variant C/T snv 8.0E-06 1
rs1330260382 1.000 0.040 4 1801390 missense variant G/A snv 6.5E-06 1
rs1555525857 1.000 0.040 17 7674935 missense variant C/A;T snv 1