Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs937475913 0.790 0.120 8 47936435 missense variant T/C snv 4.0E-06 7
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37