Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs774188914 0.851 0.200 13 102858296 missense variant C/G snv 2.4E-05 1.4E-05 4
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1799794 0.763 0.320 14 103712930 splice region variant T/C snv 0.22 12
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1805329 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 15
rs1805388 0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs7086803 0.763 0.160 10 112738717 intron variant G/A snv 0.20 9
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1537514 0.882 0.120 1 11788011 missense variant G/C snv 0.10 0.10 4