Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 3
rs8170 0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 3
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 3
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 3
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 2
rs2363956 0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 2
rs2153271 0.925 0.160 9 16864523 intron variant C/T snv 0.43 2
rs367899983 1.000 0.120 9 16864524 intron variant GTCT/- delins 4.2E-05 2
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 2
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 2
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 2
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 2
rs11651755 0.763 0.160 17 37739849 intron variant T/C snv 0.52 2
rs10810666 1.000 0.120 9 16911668 intergenic variant C/T snv 0.14 1
rs10962656 1.000 0.120 9 16877790 intergenic variant G/A snv 0.10 1
rs4445329 1.000 0.120 9 16911759 intergenic variant G/A;C snv 1
rs67397200 0.827 0.160 19 17290595 upstream gene variant C/G snv 0.27 1
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 1
rs10756819 1.000 0.120 9 16858086 intron variant G/A;C;T snv 1
rs12379183 1.000 0.120 9 16865701 intron variant A/G snv 0.26 1