Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs4647924 0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 49
rs121918459 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs1557036768 0.708 0.320 X 53647390 missense variant C/T snv 44
rs886041065 0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs886039469 0.701 0.560 10 76891709 missense variant T/C snv 35
rs387907144 0.716 0.600 6 157181056 stop gained C/A;T snv 34
rs1331463984 0.701 0.240 16 2176350 missense variant G/A snv 33
rs397517148 0.776 0.200 2 39023128 missense variant C/T snv 27
rs1554208945 0.752 0.240 6 87260207 missense variant A/C snv 26
rs1064796765 0.763 0.240 14 102002950 missense variant G/A snv 19
rs1564421528
WAC
0.882 0.080 10 28614666 stop gained C/T snv 16
rs149830411 0.827 0.360 17 46171276 stop gained G/A snv 5.2E-05 5.6E-05 15
rs1554110735 0.776 0.200 6 10398693 frameshift variant TT/- delins 13
rs200426926 0.776 0.400 16 3027379 missense variant G/A;T snv 1.8E-04; 4.0E-06 13
rs138632121 0.776 0.400 16 3026140 missense variant T/A snv 1.7E-04 2.0E-04 13
rs199473457 0.827 0.200 11 2572020 missense variant C/A;T snv 12
rs1567010427 0.882 14 102010824 missense variant G/A snv 11
rs1563005360 0.807 0.120 7 128857103 splice acceptor variant ACCTCTGGCCCCCAGGTGTGTCATCAGAGTTCATCGTGAACACCCTGAATGCCGGCTCGGGGGCCTTGTCTGTCACCATTGATGGCCCCTC/GAGG delins 11
rs886041095 0.827 0.160 12 13571930 missense variant C/T snv 11
rs1131692229 0.851 0.120 2 8730956 frameshift variant GT/- delins 11
rs1114167291 0.790 0.280 16 89281225 stop gained C/A snv 10
rs1554844486 0.827 0.160 10 75024984 frameshift variant GGGT/- del 10
rs1057516044 0.851 0.240 12 21913005 missense variant A/G snv 9