Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11249433 0.827 0.160 1 121538815 intron variant A/C;G snv 9
rs4784227 0.807 0.160 16 52565276 intron variant C/T snv 0.20 8
rs13283662 0.925 0.080 9 6428530 intron variant T/C snv 4
rs2306969 0.925 0.040 19 5851790 intron variant A/G snv 0.76 4
rs17506395 0.925 0.080 3 189803530 intron variant T/G snv 0.19 3
rs2787486 0.925 0.080 17 55132413 intron variant A/C snv 0.33 3
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs7716600 0.925 0.080 5 44874903 regulatory region variant A/C;T snv 4
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs121909219 0.689 0.400 10 87957915 stop gained C/A;T snv 25
rs786201059 0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs80358920 0.732 0.400 13 32346841 stop gained C/G;T snv 14
rs80359212 0.763 0.320 13 32394814 stop gained C/T snv 1.2E-05 4.2E-05 11
rs80358427 0.776 0.280 13 32332877 stop gained A/T snv 4.0E-06 10
rs80358785 0.790 0.240 13 32340000 stop gained C/A;G snv 1.6E-05 9
rs62625308 0.851 0.200 17 43091924 stop gained G/A;C snv 1.2E-05 8
rs80356962 0.807 0.200 17 43047666 stop gained C/G;T snv 4.0E-06 7.0E-06 8
rs80357086 0.851 0.200 17 43106480 stop gained A/G;T snv 8
rs80356978 0.827 0.200 17 43092809 stop gained C/A;T snv 7
rs80357123 0.827 0.200 17 43057078 stop gained G/A;C;T snv 1.2E-05 7
rs80358981 0.827 0.200 13 32356550 stop gained C/T snv 2.0E-05 1.4E-05 7
rs41293465 0.851 0.200 17 43045767 stop gained G/A snv 1.2E-05 6
rs80356923 0.882 0.200 17 43091891 stop gained C/A;T snv 9.9E-05 5
rs80357481 0.882 0.200 17 43094317 stop gained G/C;T snv 5