Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs1063538 1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55 4
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs12916 0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs1892534 0.925 0.120 1 65640261 3 prime UTR variant C/T snv 0.44 7
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs10895068 0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs1799941 0.763 0.280 17 7630105 5 prime UTR variant G/A snv 0.18 11
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
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43