Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs376612295 1.000 0.080 1 237454494 missense variant C/G snv 1.0E-04 7.0E-05 1
rs79457258 1.000 0.080 1 237550629 missense variant G/A;C snv 8.4E-05 1
rs769219555 0.925 0.120 1 237648612 missense variant C/T snv 4.2E-05 8.4E-05 2
rs189345192 1.000 0.080 1 237792207 missense variant G/A;C;T snv 3.6E-05 1
rs759830423 1.000 0.080 1 237445447 missense variant C/T snv 2.0E-05 2.1E-05 1
rs121918604 0.882 0.080 1 237798037 missense variant G/A;T snv 1.7E-05 3
rs753733164 1.000 0.080 1 237784887 missense variant A/G snv 1.6E-05 2.8E-05 1
rs190140598 0.851 0.120 1 237445488 missense variant C/A;T snv 1.2E-05 4
rs764772142 0.925 0.080 1 237377349 missense variant C/A;T snv 8.0E-06 2
rs371121679 1.000 0.080 1 237445471 missense variant G/A;T snv 8.0E-06 1
rs730880191 1.000 0.080 1 237566623 missense variant G/A snv 8.0E-06; 4.0E-06 1
rs1239093704 1.000 0.080 1 237759849 missense variant G/T snv 4.0E-06 1
rs730880196 1.000 0.080 1 237784037 missense variant A/C;G snv 4.0E-06 1
rs772220753 1.000 0.080 1 237640956 missense variant A/G snv 4.0E-06 1
rs1060500142 1.000 0.080 1 237330939 missense variant C/T snv 4.0E-06 1
rs794728708 0.827 0.120 1 237377386 missense variant G/A;T snv 8
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
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
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
rs121918597 0.925 0.080 1 237634937 missense variant C/T snv 2