Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs60682848 0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 11
rs80338777 0.827 0.200 1 201077915 missense variant C/A;T snv 1.2E-05 10
rs3766871 0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 9
rs794728708 0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs58327533 1.000 0.120 1 156114991 missense variant C/G;T snv 4
rs121918602 0.925 0.120 1 237454396 missense variant T/C snv 3
rs121918606 0.925 0.080 1 237819181 missense variant C/G snv 3
rs794728721 0.925 0.080 1 237445489 missense variant G/A snv 3
rs779640835 1.000 0.040 1 237566723 missense variant C/A;T snv 4.0E-06; 2.8E-05 2
rs79023478 1.000 0.040 1 228315865 missense variant G/A snv 8.4E-03 3.0E-02 2
rs1339374391 1 156135973 synonymous variant C/T snv 4.0E-06 1
rs137854618 0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 15
rs7626962 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs199473605 0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 7
rs199473225 0.851 0.120 3 38560397 missense variant G/A;C snv 6
rs137854602 0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 5
rs137854606 0.882 0.120 3 38604062 missense variant C/A snv 4
rs199473604 0.882 0.120 3 38560394 missense variant G/T snv 4
rs104893714 0.925 0.120 3 8745701 missense variant T/G snv 3
rs199473631 0.925 0.120 3 38551085 missense variant C/T snv 3
rs45627438 0.925 0.080 3 38604025 missense variant C/T snv 5.8E-05 2.8E-05 3
rs137854605 1.000 0.120 3 38581337 missense variant GA/TT mnv 2
rs184442491 1.000 0.120 3 38603888 missense variant C/A snv 2.1E-04 7.7E-04 2
rs199473142 1.000 0.120 3 38597952 missense variant C/T snv 2.1E-05 2
rs199473256 1.000 0.120 3 38556460 missense variant A/C;G snv 2