Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs132770 0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs851797 0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs34330 0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 15
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs5751129 0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs4796793 0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 16
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs1776148 0.807 0.160 1 241879243 missense variant A/G snv 0.66 0.66 9
rs664677
ATM
0.807 0.160 11 108272455 intron variant C/A;T snv 0.65 8
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs2853677 0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25