Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61753219 0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05 64
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 62
rs1010184002 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs796052243 0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs1553621496 0.677 0.440 2 209976305 splice donor variant T/G snv 53
rs1569355102 0.695 0.360 21 37472869 frameshift variant TAAC/- delins 51
rs780533096 0.701 0.600 13 23886338 missense variant C/G;T snv 4.8E-06; 9.6E-06 44
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
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
rs1554389088 0.807 0.160 7 44243526 missense variant G/A snv 27
rs374052333 0.763 0.320 3 132671032 stop gained C/G;T snv 4.0E-06 27
rs398124401 0.695 0.480 4 55346393 stop gained G/A snv 1.2E-04 2.8E-05 25
rs559979281 0.742 0.440 2 121530892 non coding transcript exon variant C/G;T snv 7.7E-06; 2.3E-05; 3.5E-04 23
rs863225422 0.742 0.440 2 121530927 non coding transcript exon variant G/A snv 4.6E-05; 7.7E-06 4.9E-05 23
rs28936415 0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs119103263 0.827 0.240 1 11992659 missense variant C/T snv 17
rs121912854 0.851 0.200 3 48592915 stop gained G/A snv 1.2E-05 7.0E-06 16
rs782736894 0.827 0.280 17 67975841 missense variant T/C;G snv 4.0E-06 7.0E-06 16
rs121912855 0.851 0.200 3 48575218 missense variant G/A snv 2.0E-05 7.0E-06 15
rs1555740650 0.807 0.240 19 49596253 stop gained G/T snv 13
rs376754460 0.807 0.280 16 8801859 missense variant G/A;C;T snv 8.0E-06 12
rs759317757 0.807 0.280 8 91078416 frameshift variant TTAAC/- delins 12