Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35385902 0.807 0.240 4 99347122 missense variant C/A;T snv 2.0E-05; 1.1E-03 9
rs1208 0.807 0.080 8 18400806 missense variant G/A;T snv 0.62; 4.0E-06 8
rs4946936 0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv 8
rs749710704 0.790 0.160 5 79119289 missense variant C/G;T snv 4.0E-06; 4.0E-06 7
rs1058172 0.882 0.080 22 42127526 missense variant C/G;T snv 4.4E-06; 9.2E-02 4
rs1629816 0.851 0.080 3 10294607 non coding transcript exon variant G/A;C snv 4
rs35431622 0.851 0.120 1 204190794 missense variant T/A;C snv 5.5E-05; 4.7E-02 4
rs4855883 0.851 0.080 3 49673881 upstream gene variant G/A;C snv 4
rs6796803 0.925 0.040 3 186746318 intron variant T/A;C snv 4
rs762384959 0.925 0.040 14 20456680 missense variant G/C snv 8.0E-06 4
rs763015080 0.851 0.120 4 147539821 missense variant G/A snv 4.1E-06 4
rs985325188 0.851 0.080 14 20456806 missense variant A/C snv 4
rs1667255 0.925 0.040 18 31607316 intergenic variant A/C;G;T snv 3
rs752153816 0.882 0.120 6 43780848 missense variant G/A;C snv 4.0E-06; 4.0E-06; 1.2E-05; 3.6E-05 3
rs876659477 0.882 0.040 17 7673730 missense variant T/C snv 3
rs1183646267
ATM
0.925 0.040 11 108281026 missense variant A/G snv 2
rs16943176 0.925 0.040 17 58692526 upstream gene variant G/A;C snv 2
rs4253132 0.925 0.040 10 49493110 splice region variant G/A;T snv 0.89; 4.4E-05 2
rs554194414 0.925 0.040 2 8731250 missense variant T/C snv 2
rs770925903 0.925 0.040 2 8731740 missense variant C/A;T snv 1.6E-05; 4.0E-06 2
rs7802034 0.925 0.040 7 152655183 intron variant A/C;G snv 2
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1297812518 0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05 9
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32