Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs879253942 0.677 0.400 17 7673826 missense variant A/G snv 28
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs333 0.667 0.520 3 46373453 frameshift variant GTCAGTATCAATTCTGGAAGAATTTCCAGACA/- delins 7.3E-02 23
rs4636297 0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs1799987 0.763 0.200 3 46370444 intron variant A/G snv 0.49 10
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs746700511 0.851 0.080 22 37665657 missense variant T/C snv 4.0E-06 4
rs3219218
UNG
0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 4
rs1800023 1.000 0.040 3 46370817 intron variant A/G snv 0.29 2