Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060500142 1.000 0.080 1 237330939 missense variant C/T snv 4.0E-06 1
rs1558698334 1.000 0.080 1 237369568 missense variant A/G snv 1
rs764772142 0.925 0.080 1 237377349 missense variant C/A;T snv 8.0E-06 2
rs397516539 1.000 0.080 1 237377365 missense variant G/A;T snv 1
rs1553426678 1.000 0.080 1 237377374 missense variant G/A snv 1
rs794728708 0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs1415931588 1.000 0.080 1 237377426 missense variant A/T snv 2
rs1458500258 0.925 0.080 1 237388098 missense variant G/T snv 7.0E-06 3
rs1401116572 1.000 0.080 1 237441382 missense variant G/A snv 2
rs1553454821 1.000 0.080 1 237445428 missense variant G/A snv 1
rs759830423 1.000 0.080 1 237445447 missense variant C/T snv 2.0E-05 2.1E-05 1
rs371121679 1.000 0.080 1 237445471 missense variant G/A;T snv 8.0E-06 1
rs1349176732 1.000 0.080 1 237445485 missense variant A/T snv 1
rs190140598 0.851 0.120 1 237445488 missense variant C/A;T snv 1.2E-05 4
rs794728721 0.925 0.080 1 237445489 missense variant G/A snv 3
rs121918602 0.925 0.120 1 237454396 missense variant T/C snv 3
rs376612295 1.000 0.080 1 237454494 missense variant C/G snv 1.0E-04 7.0E-05 1
rs730880187 1.000 0.080 1 237492973 missense variant C/T snv 1
rs79457258 1.000 0.080 1 237550629 missense variant G/A;C snv 8.4E-05 1
rs730880191 1.000 0.080 1 237566623 missense variant G/A snv 8.0E-06; 4.0E-06 1
rs1553531703 1.000 0.080 1 237628052 missense variant G/A snv 1
rs1558103974 1.000 0.080 1 237633668 missense variant G/C snv 1
rs121918597 0.925 0.080 1 237634937 missense variant C/T snv 2
rs794728746 1.000 0.080 1 237638480 missense variant G/A;C snv 1
rs794728747 1.000 0.080 1 237639019 missense variant G/T snv 1