Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4430796 0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182