Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 91
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs228593
ATM
11 108270407 intron variant G/A snv 0.27 1
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 14
rs3835 0.882 0.120 2 216201914 intron variant G/A snv 0.21 4
rs2228526 0.752 0.200 10 49470671 missense variant T/C snv 0.22 0.19 13
rs2228529 0.925 0.080 10 49459059 missense variant T/C snv 0.22 0.19 4
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 47
rs2230641 0.807 0.240 5 87399457 missense variant A/G;T snv 0.18 0.17 7
rs1805388 0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11
rs4553808 0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 53
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 14
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 201
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs2308327 0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02 10
rs1800067 0.716 0.320 16 13935176 missense variant G/A snv 5.6E-02 5.3E-02 17
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 230
rs8179090 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 12
rs3746609 20 32434666 missense variant G/A snv 1.9E-02; 4.4E-06 7.4E-03 1
rs118101777 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs72661120 17 7673717 synonymous variant T/C snv 2.7E-04 7.0E-05 1
rs927698341 0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10