Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6590811 | 11 | 100708153 | intron variant | C/T | snv | 0.53 | 4 | ||||
rs6590812 | 11 | 100711497 | intron variant | G/A | snv | 0.55 | 1 | ||||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 10 | |||
rs6590816 | 11 | 100730902 | intron variant | G/A | snv | 0.40 | 4 | ||||
rs604723 | 1.000 | 0.040 | 11 | 100739815 | intron variant | T/C | snv | 0.78 | 9 | ||
rs7801190 | 1.000 | 0.040 | 7 | 100860471 | non coding transcript exon variant | C/G | snv | 9.9E-02 | 2 | ||
rs104893831 | 0.925 | 0.040 | 3 | 10146549 | missense variant | G/A;C;T | snv | 2.0E-05 | 2 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 30 | ||
rs11568818 | 0.763 | 0.280 | 11 | 102530930 | upstream gene variant | T/A;C | snv | 2 | |||
rs104894145 | 0.925 | 0.240 | 10 | 102830946 | missense variant | G/A | snv | 1 | |||
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 8 | |
rs4919687 | 0.742 | 0.160 | 10 | 102835491 | non coding transcript exon variant | G/A | snv | 0.25 | 9 | ||
rs13175330 | 5 | 102840757 | intron variant | A/G | snv | 7.8E-02 | 1 | ||||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 2 | |
rs4409766 | 1.000 | 0.040 | 10 | 102856906 | intron variant | T/C | snv | 0.14 | 6 | ||
rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 2 | |
rs34911341 | 0.882 | 0.200 | 3 | 10289835 | missense variant | C/T | snv | 7.0E-03 | 7.3E-03 | 2 | |
rs12413409 | 0.790 | 0.200 | 10 | 102959339 | intron variant | G/A | snv | 9.0E-02 | 6 | ||
rs11191514 | 10 | 103013607 | intron variant | C/G;T | snv | 1 | |||||
rs11191548 | 0.882 | 0.080 | 10 | 103086421 | 3 prime UTR variant | T/C | snv | 8.6E-02 | 7 | ||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 12 | ||
rs12219304 | 10 | 103171827 | intron variant | G/C;T | snv | 1 | |||||
rs11191593 | 10 | 103179458 | intron variant | T/C | snv | 9.0E-02 | 4 | ||||
rs112913898 | 10 | 103199143 | intergenic variant | G/A | snv | 9.1E-02 | 3 | ||||
rs4387287 | 10 | 103918139 | 5 prime UTR variant | A/C | snv | 0.69 | 3 |