Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777893 0.658 0.240 1 11128107 missense variant G/A;T snv 67
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs1560755661 0.701 0.480 4 106171094 splice donor variant CAGATCTGTCTTTGGAGGATCTGGACACTCAGCAGAGAAATAAGGTGCCGAACTTCTGCCTCCACTGCTGTCAGAAGATGGCTTTGGAGGTTGAGCATGCTGTCTGTAAGTAGCACTTTTAGGAGTCCAACAAAACAGGTTGATAGATTCTCTCACACAGCGTTCAATGTCAATTTC/- delins 44
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs1553770577 0.724 0.480 3 132675342 missense variant T/C snv 37
rs878853250 0.752 0.360 12 51699663 stop gained T/A;C snv 37
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
rs1057524157 0.776 0.200 11 686962 missense variant A/C;T snv 19
rs1057519565 0.851 0.200 11 687941 missense variant C/T snv 9