Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs794728708 0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs267607277 0.807 0.120 14 90404386 missense variant A/G snv 6
rs398124647 0.807 0.120 2 47161851 missense variant T/A;C snv 6
rs121918600 0.882 0.080 1 237791441 missense variant C/T snv 5
rs121918598 0.851 0.080 1 237648523 missense variant G/A;C snv 4
rs190140598 0.851 0.120 1 237445488 missense variant C/A;T snv 1.2E-05 4
rs11551437 1.000 0.080 2 47161833 missense variant G/A snv 3
rs398124650 0.882 0.120 2 47161744 missense variant C/G;T snv 3
rs749547712 0.882 0.080 1 115768444 missense variant C/T snv 1.2E-05 3
rs121918602 0.925 0.120 1 237454396 missense variant T/C snv 3
rs121918603 0.882 0.080 1 237639068 missense variant C/T snv 3
rs121918604 0.882 0.080 1 237798037 missense variant G/A;T snv 1.7E-05 3
rs121918606 0.925 0.080 1 237819181 missense variant C/G snv 3
rs1273246817 0.882 0.080 1 237784169 missense variant A/C snv 3
rs1458500258 0.925 0.080 1 237388098 missense variant G/T snv 7.0E-06 3
rs794728721 0.925 0.080 1 237445489 missense variant G/A snv 3
rs773204795 0.882 0.120 4 64309896 missense variant C/T snv 2.4E-05 2.1E-05 3
rs397515458 0.925 0.080 6 123503899 stop gained G/A snv 3.1E-05 5.6E-05 3
rs267607276 0.925 0.080 14 90401385 missense variant A/G;T snv 2
rs398124648 0.925 0.080 2 47161748 missense variant A/C snv 2
rs398124649 0.925 0.080 2 47161737 missense variant T/G snv 2
rs121434549 0.925 0.080 1 115705212 missense variant C/G;T snv 8.0E-06 2
rs121434550 0.925 0.080 1 115738256 missense variant A/T snv 2
rs886039816 0.925 0.080 1 115732968 missense variant T/C snv 2
rs768049331 0.925 0.080 6 123571099 frameshift variant GTCT/- delins 2.8E-05 2.2E-04 2