Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1163944538 0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1352010373 0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs587777893 0.658 0.240 1 11128107 missense variant G/A;T snv 67
rs1276519904 0.645 0.520 1 226071445 missense variant A/G snv 63
rs779027563 0.677 0.360 17 42687838 missense variant G/C snv 4.0E-06 7.0E-06 58
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs61750420 0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 52
rs4647924 0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 49
rs200661329 0.708 0.440 16 576255 splice donor variant G/A;C snv 5.7E-05 48
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs1400419650 0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 38
rs1555386022 0.708 0.320 14 92003418 splice donor variant C/A snv 38
rs80338945 0.695 0.440 13 20189313 missense variant A/G snv 6.4E-04 6.4E-04 32
rs149617956 0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 32
rs66527965 0.763 0.240 17 50193038 missense variant C/A;T snv 31
rs312262690 0.752 0.320 4 79984831 frameshift variant -/G;GG delins 1.7E-05 28
rs397517148 0.776 0.200 2 39023128 missense variant C/T snv 27
rs1559470315 0.732 0.320 3 41227287 protein altering variant CCACAAGCAG/T delins 26
rs121908557 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 23
rs387907260 0.776 0.280 7 66633410 missense variant C/T snv 4.0E-06 1.4E-05 22
rs796052686 0.776 0.280 7 66638394 missense variant G/A snv 1.2E-05 22
rs864309486 0.763 0.320 6 24777262 stop gained A/T snv 21
rs1558373252 0.790 0.120 2 5693013 frameshift variant T/- delins 19
rs1553212868 0.807 0.280 1 151406264 frameshift variant G/- delins 17
rs912001256 0.851 0.240 17 63947062 stop gained G/A snv 17