Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 62
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
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs878853250 0.752 0.360 12 51699663 stop gained T/A;C snv 37
rs387907145 0.695 0.440 16 4800548 stop gained G/A snv 35
rs786205124 0.701 0.400 16 4798593 frameshift variant G/-;GGG delins 3.5E-05 35
rs374052333 0.763 0.320 3 132671032 stop gained C/G;T snv 4.0E-06 27
rs77078070 0.742 0.280 7 23165737 stop gained C/T snv 1.2E-05 1.4E-05 26
rs886041091 0.807 0.120 9 84751990 missense variant A/G snv 18
rs1057516033 0.807 0.400 10 75025250 splice donor variant G/A snv 9
rs1057516049 0.851 0.040 8 41933963 frameshift variant CACT/- delins 7