Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs61755320 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 41
rs1345176461 0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs878853250 0.752 0.360 12 51699663 stop gained T/A;C snv 37
rs387907145 0.695 0.440 16 4800548 stop gained G/A snv 36
rs786205124 0.701 0.400 16 4798593 frameshift variant G/-;GGG delins 3.5E-05 35
rs374052333 0.763 0.320 3 132671032 stop gained C/G;T snv 4.0E-06 27
rs375817528 0.776 0.160 11 65206824 splice region variant G/A snv 1.2E-04 1.2E-04 25
rs758361736 0.776 0.240 15 89649836 missense variant T/G snv 1.3E-05 1.4E-05 16
rs1217391623 0.882 0.160 16 89556976 frameshift variant G/- del 7.0E-06 11
rs121918358 0.882 0.160 16 89510539 stop gained T/A snv 4.2E-04 1.8E-04 5
rs141659620 0.882 0.160 16 89531961 missense variant G/A;C snv 8.3E-04; 8.0E-06 5
rs72547551 0.882 0.160 16 89550545 missense variant C/T snv 3.6E-05 1.5E-04 5
rs748309520 0.882 0.160 16 89531903 splice acceptor variant G/A snv 1.6E-05 7.0E-06 5
rs752989523 0.882 0.160 16 89553853 stop gained G/A;C snv 8.0E-06 5
rs879253797 0.882 0.160 16 89556954 missense variant C/T snv 1.4E-05 5