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
rs1557781252 0.742 0.320 1 153816414 stop gained G/A snv 33
rs387906846 0.807 0.280 1 26773716 stop gained C/G;T snv 19
rs1553212868 0.807 0.280 1 151406264 frameshift variant G/- delins 17
rs794727774 0.827 0.240 1 23848684 stop gained C/T snv 11
rs375761808 0.925 0.160 1 26775673 missense variant A/G;T snv 4.0E-06 6
rs587779388 1.000 1 113898755 frameshift variant GT/- delins 1.4E-04 1.5E-04 5
rs1553621496 0.677 0.440 2 209976305 splice donor variant T/G snv 53
rs1553511224 0.882 0.080 2 161423825 frameshift variant -/C delins 10
rs879253767 0.882 0.080 2 165313738 frameshift variant T/- delins 6
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs1553770577 0.724 0.480 3 132675342 missense variant T/C snv 37
rs1559759089 0.827 0.200 3 113795101 missense variant C/A snv 14
rs1553632357 0.882 0.120 3 41236421 stop gained G/T snv 5
rs1560755661 0.701 0.480 4 106171094 splice donor variant CAGATCTGTCTTTGGAGGATCTGGACACTCAGCAGAGAAATAAGGTGCCGAACTTCTGCCTCCACTGCTGTCAGAAGATGGCTTTGGAGGTTGAGCATGCTGTCTGTAAGTAGCACTTTTAGGAGTCCAACAAAACAGGTTGATAGATTCTCTCACACAGCGTTCAATGTCAATTTC/- delins 44
rs372392424 0.882 0.240 4 523849 missense variant C/T snv 6.7E-05 7.7E-05 8
rs796052505 0.724 0.440 5 162095551 missense variant G/A;C snv 57
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs1131692231 0.827 0.280 5 157294834 missense variant C/T snv 13
rs879253745 0.925 0.240 6 157181040 frameshift variant AA/- delins 6
rs879253746 0.925 0.240 6 157200866 frameshift variant -/T delins 6
rs879253747 0.925 0.240 6 157167101 stop gained C/T snv 6
rs879253856 0.925 0.240 6 157110496 frameshift variant CCG/TCCGCAGCCACTCC delins 6
rs1057518796 1.000 6 33443751 frameshift variant C/- delins 3
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54