Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140511594 0.742 0.360 2 165941111 missense variant G/A snv 1.3E-04 1.1E-04 13
rs1131692245 0.925 0.160 19 35844109 missense variant C/T snv 7
rs386833945 0.882 0.080 19 35850987 missense variant G/A snv 4
rs114896482 0.882 0.080 19 35842487 missense variant G/A snv 2.3E-03 1.5E-03 3
rs28939378 0.925 0.160 16 5078789 missense variant C/T snv 3.0E-04 3.5E-04 3
rs267606919 1.000 0.080 19 35831056 stop gained G/A snv 9.9E-05 2
rs386833895 0.925 0.080 19 35845430 missense variant C/A snv 3.6E-05 7.0E-05 2
rs763972372 0.925 0.080 19 35849060 missense variant C/T snv 1.2E-05 2.1E-05 2
rs1009762900 1.000 0.080 19 35831763 splice acceptor variant C/A;T snv 1
rs1054950770 1.000 0.080 19 35851260 splice donor variant A/G snv 7.0E-06 1
rs1057516776 1.000 0.080 19 35848147 stop gained C/T snv 1
rs1057517413 1.000 0.080 19 35848795 splice acceptor variant C/G snv 1
rs113825926 1.000 0.080 19 35849107 missense variant G/A snv 7.7E-03 8.5E-03 1
rs114203578 1.000 0.080 19 35842480 missense variant C/G;T snv 6.8E-05 1
rs114849139 1.000 0.080 19 35839554 missense variant C/G;T snv 1.1E-03; 8.0E-05 1
rs137853042 1.000 0.080 19 35831358 stop gained G/A snv 1.6E-04 2.1E-05 1
rs138656762 1.000 0.080 19 35839418 missense variant C/A snv 4.4E-05 4.2E-05 1
rs139598219 1.000 0.080 19 35850407 stop gained C/A;T snv 7.2E-05 1
rs140018064 1.000 0.080 19 35842406 stop gained G/A;T snv 2.0E-05 1
rs142008044 1.000 0.080 19 35848334 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 5.2E-05 1
rs143092783 1.000 0.080 19 35831116 missense variant G/A;T snv 1.0E-04; 9.8E-04 1
rs143649022 1.000 0.080 19 35841802 missense variant A/G snv 4.0E-06 2.8E-05 1
rs145125791 1.000 0.080 19 35850409 missense variant T/A snv 6.0E-03 6.0E-03 1
rs1468337078 1.000 0.080 19 35845727 missense variant A/T snv 7.0E-06 1
rs150038620 1.000 0.080 19 35842551 splice acceptor variant C/T snv 9.2E-05 9.1E-05 1