Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | |||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs121912438 | 0.605 | 0.520 | 21 | 31667299 | missense variant | G/A;C;T | snv | 1.2E-05; 8.0E-06 | 58 | ||
rs397517132 | 0.623 | 0.280 | 7 | 55191846 | missense variant | A/T | snv | 48 | |||
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 | |
rs2234767 | 0.649 | 0.280 | 10 | 88989499 | intron variant | G/A;T | snv | 0.15 | 30 | ||
rs281865545 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 18 | |||
rs16754 | 0.732 | 0.240 | 11 | 32396399 | synonymous variant | T/C | snv | 0.24; 4.0E-06 | 0.17 | 15 | |
rs10821936 | 0.742 | 0.200 | 10 | 61963818 | intron variant | C/T | snv | 0.69 | 11 | ||
rs7089424 | 0.752 | 0.200 | 10 | 61992400 | intron variant | T/G | snv | 0.32 | 10 | ||
rs41293463 | 0.790 | 0.280 | 17 | 43051071 | missense variant | A/C;T | snv | 1.2E-05 | 9 | ||
rs1057519753 | 0.763 | 0.120 | 1 | 64846664 | missense variant | C/A | snv | 9 | |||
rs11191439 | 0.851 | 0.120 | 10 | 102878966 | missense variant | T/A;C | snv | 9.2E-02 | 6 | ||
rs10748835 | 0.827 | 0.160 | 10 | 102900499 | non coding transcript exon variant | G/A | snv | 0.41 | 5 | ||
rs7560488 | 0.851 | 0.160 | 2 | 25345952 | upstream gene variant | T/C | snv | 0.40 | 4 | ||
rs7073837 | 0.851 | 0.120 | 10 | 61940136 | intron variant | A/C | snv | 0.58 | 0.64 | 4 | |
rs2393726 | 0.925 | 0.040 | 10 | 62094648 | 3 prime UTR variant | A/G | snv | 3.9E-02 | 2 | ||
rs6415872 | 0.925 | 0.040 | 10 | 61900930 | upstream gene variant | G/A | snv | 0.51 | 2 | ||
rs3740390 | 0.925 | 0.080 | 10 | 102878723 | intron variant | C/T | snv | 9.2E-02 | 2 | ||
rs11191453 | 1.000 | 0.040 | 10 | 102900095 | intron variant | T/C | snv | 9.0E-02 | 1 |