Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs756851968 1.000 0.080 8 60741555 missense variant G/A snv 1.2E-05 1.4E-05 1
rs767819417 1.000 0.080 8 60741647 missense variant A/G snv 1.2E-05 2.1E-05 1
rs779024959 1.000 0.080 8 60741727 missense variant G/A;C snv 4.8E-05; 3.2E-05 1
rs200898742 1.000 0.080 8 60742144 missense variant G/A;C snv 3.4E-04; 4.0E-06 1
rs772369092 1.000 0.080 8 60742747 missense variant C/G;T snv 1.6E-05; 4.0E-06 1
rs746837682 1.000 0.080 8 60781006 missense variant C/G snv 6.4E-05 7.0E-05 1
rs756365280 1.000 0.080 8 60795071 missense variant G/A;C snv 2.4E-05; 6.4E-05 1
rs121434344 0.882 0.080 8 60816389 missense variant C/T snv 1
rs377662366 1.000 0.080 8 60820073 missense variant A/C;G snv 3.3E-03 1
rs1165711448 1.000 0.080 8 60821842 missense variant C/T snv 1
rs763978472 1.000 0.080 8 60821905 missense variant G/A;C snv 4.0E-06; 4.0E-06 1
rs370194460 1.000 0.080 8 60821916 missense variant A/G snv 1.4E-04 2.1E-05 1
rs117506164 1.000 0.080 8 60821923 missense variant G/A snv 6.1E-04 2.9E-04 1
rs768481542 1.000 0.080 8 60822028 missense variant G/A snv 7.6E-05 4.2E-05 1
rs1057521077 1.000 0.080 8 60822604 missense variant T/C snv 1
rs121434338 0.925 0.080 8 60822627 missense variant A/G snv 1
rs886040988 1.000 0.080 8 60830422 missense variant T/A snv 1
rs121434339 1.000 0.080 8 60830569 missense variant T/G snv 1
rs864309609 1.000 0.080 8 60836175 missense variant T/C snv 1
rs373301291 1.000 0.080 8 60836243 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 4.0E-05 1
rs770166812 1.000 0.080 8 60837729 missense variant C/G;T snv 4.2E-06 1
rs773187713 1.000 0.080 8 60841976 missense variant C/T snv 1.6E-05 7.0E-06 1
rs886040993 1.000 0.080 8 60842051 missense variant G/A snv 1
rs1554602465 0.882 0.080 8 60845063 missense variant G/A snv 2
rs201423234 1.000 0.080 8 60852201 missense variant G/A snv 2.3E-04 2.2E-04 1