Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143456784 1.000 0.120 7 117504324 missense variant C/T snv 1.2E-04 7.7E-05 1
rs121908759 0.827 0.160 7 117592032 missense variant G/A snv 1.0E-04 3.8E-04 1
rs397508276 0.925 0.160 7 117590378 missense variant T/C;G snv 9.6E-05 1
rs121908755 0.882 0.200 7 117587800 missense variant G/A;T snv 8.8E-05 1
rs151048781 0.925 0.160 7 117603730 missense variant G/A;C snv 5.6E-05; 8.0E-05 2
rs145540754 1.000 0.120 7 117592246 missense variant T/G snv 7.2E-05; 8.0E-06 3.1E-04 1
rs74551128 0.807 0.160 7 117548795 missense variant C/A;T snv 5.3E-05; 5.7E-05 1
rs149353983 1.000 0.120 7 117504291 missense variant G/A;T snv 5.6E-05; 3.2E-05 1
rs121909011 0.807 0.160 7 117540230 missense variant C/T snv 5.6E-05 9.1E-05 2
rs193922506 1.000 0.120 7 117595036 missense variant G/A snv 4.8E-05 4.9E-05 1
rs75961395 0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 1
rs368505753 0.925 0.160 7 117509069 missense variant C/T snv 3.6E-05 3.5E-05 1
rs397508553 1.000 0.120 7 117614654 missense variant A/G snv 3.6E-05 4.9E-05 1
rs78194216 0.925 0.160 7 117611637 missense variant C/A;T snv 3.2E-05 1
rs121909019 0.925 0.160 7 117611638 missense variant G/A;T snv 3.2E-05 1
rs780526529 1.000 0.120 7 117592118 missense variant G/A snv 3.2E-05 1
rs193922516 1.000 0.120 7 117610568 missense variant C/A;G;T snv 3.2E-05; 4.0E-06; 3.2E-05 1
rs201124247 0.882 0.160 7 117592008 missense variant A/G snv 3.1E-05 1
rs77409459 0.851 0.160 7 117540243 missense variant C/T snv 2.8E-05 1.4E-05 1
rs80055610 0.851 0.160 7 117587833 missense variant G/A;C snv 2.4E-05 1
rs121908753 0.851 0.160 7 117540285 missense variant G/A snv 2.4E-05 1
rs77932196 0.790 0.280 7 117540270 missense variant G/A;C;T snv 2.4E-05; 2.4E-05 1
rs397508783 0.925 0.160 7 117535363 missense variant T/A snv 2.4E-05 7.0E-06 1
rs139468767 0.925 0.160 7 117592020 missense variant T/C snv 2.2E-05 1.6E-04 1
rs75549581 0.925 0.160 7 117587829 missense variant G/A;T snv 2.0E-05; 4.0E-06 1