Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770374710 0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs1555743003 0.701 0.520 18 33740444 splice donor variant G/A snv 58
rs200661329 0.708 0.440 16 576255 splice donor variant G/A;C snv 5.7E-05 48
rs1560755661 0.701 0.480 4 106171094 splice donor variant CAGATCTGTCTTTGGAGGATCTGGACACTCAGCAGAGAAATAAGGTGCCGAACTTCTGCCTCCACTGCTGTCAGAAGATGGCTTTGGAGGTTGAGCATGCTGTCTGTAAGTAGCACTTTTAGGAGTCCAACAAAACAGGTTGATAGATTCTCTCACACAGCGTTCAATGTCAATTTC/- delins 44
rs1364709483 0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05 36
rs369160589 0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04 35
rs1009298200 0.742 0.400 16 5079077 missense variant C/G;T snv 7.0E-06 34
rs1555452127 0.742 0.400 16 5079078 missense variant T/C snv 34
rs1557781252 0.742 0.320 1 153816414 stop gained G/A snv 33
rs1563183492 0.708 0.520 7 70766248 missense variant C/T snv 32
rs1421405659 0.851 0.360 12 101642529 missense variant T/C;G snv 13