Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554121443 0.742 0.280 6 33438873 stop gained C/T snv 29
rs201893408 0.695 0.480 8 93795970 missense variant T/A;C snv 8.0E-06; 1.5E-04 28
rs1554389088 0.807 0.160 7 44243526 missense variant G/A snv 27
rs387907141 0.752 0.360 6 157181137 stop gained C/T snv 24
rs1448259271 0.790 0.240 14 77027279 stop gained C/A;T snv 23
rs1555429629 0.763 0.200 15 40729632 missense variant G/A snv 23
rs1555745467 0.752 0.240 19 13262771 missense variant C/A snv 23
rs559979281 0.742 0.440 2 121530892 non coding transcript exon variant C/G;T snv 7.7E-06; 2.3E-05; 3.5E-04 23
rs863225422 0.742 0.440 2 121530927 non coding transcript exon variant G/A snv 4.6E-05; 7.7E-06 4.9E-05 23
rs28936415 0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs121913348 0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs398123009 0.790 0.200 11 66211206 missense variant C/T snv 7.0E-06 19
rs61750240 0.752 0.240 X 154031020 stop gained G/A;C snv 5.5E-06 19
rs1555377415 0.827 0.200 14 77027274 stop gained G/C snv 18
rs606231435 0.827 0.240 19 41970539 missense variant C/T snv 18
rs137852832 0.716 0.280 12 88077263 stop gained C/A snv 9.5E-05 6.3E-05 17
rs398122394 0.763 0.240 X 111685040 missense variant A/G snv 17
rs61749721 0.732 0.200 X 154031065 stop gained G/A snv 17
rs797044849 0.807 0.160 12 13567164 missense variant C/A;G;T snv 4.0E-06 17
rs80356537 0.752 0.320 19 41970405 missense variant C/A;G;T snv 17
rs267607048 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 16
rs387906702 0.807 0.200 X 53403635 missense variant A/G snv 16
rs759125480 0.827 0.160 5 123377409 stop gained G/A snv 1.6E-05 16
rs147001633 0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04 15
rs149830411 0.827 0.360 17 46171276 stop gained G/A snv 5.2E-05 5.6E-05 15