Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs727505375 1.000 0.040 4 103658329 stop gained C/T snv 4.0E-06 7.0E-06 1
rs727505377 1.000 0.040 8 38414001 missense variant A/G snv 1
rs774317793 1.000 0.040 4 67754283 missense variant T/C snv 1.9E-04 2.1E-05 1
rs797044452 1.000 0.040 4 67744788 splice acceptor variant C/T snv 1
rs886907903 1.000 0.040 4 67754226 missense variant A/C snv 1
rs1057518936 0.925 0.120 19 7541025 missense variant C/G snv 3
rs121909628 0.925 0.160 8 38414892 stop gained G/A;C snv 3
rs727505369 0.925 0.160 8 38424624 missense variant T/C snv 3
rs727505373 0.925 0.160 8 38429744 missense variant T/C snv 3
rs104893836 0.790 0.160 4 67754019 missense variant T/C snv 2.8E-03 2.3E-03 2
rs727505376 0.925 0.160 8 38414279 missense variant C/G;T snv 2
rs730882248 0.925 0.160 7 5711761 splice region variant C/T snv 2
rs876661330 0.882 0.160 10 101771522 stop gained G/A snv 4.0E-06 2
rs104893837 0.807 0.160 4 67740682 missense variant C/T snv 1.8E-03 1.3E-03 1
rs104893844 0.882 0.160 4 67754068 missense variant C/T snv 3.6E-05 7.0E-06 1
rs121909640 0.925 0.160 8 38429898 missense variant C/T snv 1
rs148499544 0.882 0.160 4 67740670 missense variant A/C snv 8.0E-06 5.6E-05 1
rs74452732 0.851 0.160 4 67753825 missense variant C/A;T snv 4.0E-06 1
rs781328162 0.925 0.160 8 38413714 missense variant C/T snv 2.0E-05 3.5E-05 1
rs374434303 0.882 0.200 19 7561509 missense variant C/A;T snv 3.8E-05 4
rs774526181 0.882 0.200 12 106427360 splice donor variant T/C snv 8.0E-06 2.1E-05 3
rs138249161 0.827 0.240 12 106432421 missense variant T/A snv 2.7E-04 3.0E-04 8
rs886039799 0.763 0.320 7 33273896 frameshift variant C/- del 17
rs515726224 0.925 0.320 8 38417962 missense variant C/T snv 3
rs121909641 0.763 0.520 8 38419720 missense variant G/A snv 9