Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs774277300 0.742 0.360 11 94447276 stop gained G/A;C;T snv 2.8E-05; 4.0E-05; 4.0E-06 17
rs1114167291 0.790 0.280 16 89281225 stop gained C/A snv 10
rs28936415 0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs376754460 0.807 0.280 16 8801859 missense variant G/A;C;T snv 8.0E-06 12
rs753635972 0.790 0.120 15 79845388 missense variant C/T snv 3.2E-05 2.1E-05 15
rs771379232 0.790 0.120 15 79845338 stop gained G/A snv 2.0E-05 3.5E-05 15
rs1448259271 0.790 0.240 14 77027279 stop gained C/A;T snv 23
rs1563183492 0.708 0.520 7 70766248 missense variant C/T snv 32
rs1057518345 0.742 0.400 20 50894172 frameshift variant ACTA/- delins 25
rs397509426 0.882 0.080 3 49723632 missense variant G/A snv 8.0E-05 7.0E-06 7
rs202160208 0.827 0.160 3 49722056 missense variant C/T snv 2.9E-04 1.8E-04 9
rs1555741826 0.776 0.280 19 49601646 frameshift variant TGCC/- delins 16
rs1557043622 0.695 0.400 X 48909843 missense variant C/A snv 46
rs776095655 0.827 0.160 1 42927684 missense variant C/A;T snv 4.0E-06 8
rs875989803 0.827 0.200 X 41343249 stop gained G/T snv 15
rs1559470315 0.732 0.320 3 41227287 protein altering variant CCACAAGCAG/T delins 26
rs142239530 0.790 0.320 11 4091328 missense variant C/G;T snv 4.4E-05 24
rs2244352 0.925 0.080 21 39386047 intron variant T/A;G snv 3
rs1568359734 0.827 0.240 18 33738903 frameshift variant A/- delins 8
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs398124204 0.925 0.160 14 28767733 frameshift variant G/-;GG delins 2
rs766858016 0.882 0.200 2 25247710 stop gained T/A;G snv 4.0E-06 4
rs780533096 0.701 0.600 13 23886338 missense variant C/G;T snv 4.8E-06; 9.6E-06 44
rs770374710 0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs1553621496 0.677 0.440 2 209976305 splice donor variant T/G snv 53