Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886039816 0.925 0.080 1 115732968 missense variant T/C snv 2
rs886039172 1.000 0.080 1 237832591 missense variant G/A;C snv 1
rs876661386 1.000 0.080 1 237792304 missense variant T/C snv 1
rs876657635 1.000 0.080 1 115702996 splice acceptor variant C/A snv 1
rs794728832 1.000 0.080 1 237832628 missense variant A/G snv 1
rs794728830 1.000 0.080 1 237792276 missense variant C/T snv 1
rs794728811 0.925 0.080 1 237832619 missense variant G/A snv 2
rs794728810 1.000 0.080 1 237832588 missense variant T/C snv 1
rs794728804 1.000 0.080 1 237808913 missense variant G/A snv 1
rs794728802 1.000 0.080 1 237806236 missense variant A/C;G snv 1
rs794728780 1.000 0.080 1 237783707 missense variant A/G;T snv 1
rs794728777 1.000 0.080 1 237778726 missense variant G/A snv 1
rs794728756 1.000 0.080 1 237640983 missense variant G/A;C;T snv 1
rs794728754 1.000 0.080 1 237640941 missense variant C/T snv 1
rs794728753 1.000 0.080 1 237640940 missense variant G/A;C snv 1
rs794728747 1.000 0.080 1 237639019 missense variant G/T snv 1
rs794728746 1.000 0.080 1 237638480 missense variant G/A;C snv 1
rs794728721 0.925 0.080 1 237445489 missense variant G/A snv 3
rs794728708 0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs79457258 1.000 0.080 1 237550629 missense variant G/A;C snv 8.4E-05 1
rs781420323 1.000 0.080 6 123255108 frameshift variant TT/- delins 2.2E-05 1.4E-05 1
rs773204795 0.882 0.120 4 64309896 missense variant C/T snv 2.4E-05 2.1E-05 3
rs772220753 1.000 0.080 1 237640956 missense variant A/G snv 4.0E-06 1
rs769219555 0.925 0.120 1 237648612 missense variant C/T snv 4.2E-05 8.4E-05 2
rs768049331 0.925 0.080 6 123571099 frameshift variant GTCT/- delins 2.8E-05 2.2E-04 2