Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2246614 | 0.882 | 0.160 | 11 | 619789 | missense variant | T/G | snv | 0.63 | 0.59 | 3 | |
rs958476 | 0.925 | 0.160 | 11 | 129451923 | 3 prime UTR variant | T/A;G | snv | 2 | |||
rs11057864 | 0.925 | 0.160 | 12 | 124851404 | intron variant | C/A | snv | 6.5E-02 | 2 | ||
rs8012283 | 0.925 | 0.160 | 14 | 50767442 | intron variant | A/G | snv | 0.23 | 2 | ||
rs61752717 | 0.583 | 0.840 | 16 | 3243407 | missense variant | T/A;C | snv | 2.8E-04 | 72 | ||
rs3743930 | 0.611 | 0.720 | 16 | 3254626 | missense variant | C/G;T | snv | 7.1E-02 | 43 | ||
rs1143679 | 0.732 | 0.520 | 16 | 31265490 | missense variant | G/A | snv | 9.7E-02 | 0.11 | 14 | |
rs28940579 | 0.732 | 0.440 | 16 | 3243310 | missense variant | A/G;T | snv | 2.2E-03; 4.0E-06 | 13 | ||
rs274068 | 0.925 | 0.160 | 16 | 24887651 | intron variant | C/A | snv | 0.74 | 2 | ||
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs8091180 | 1.000 | 0.160 | 18 | 79404243 | intron variant | G/A | snv | 0.46 | 3 | ||
rs3746444 | 0.514 | 0.760 | 20 | 34990448 | mature miRNA variant | A/G | snv | 0.20 | 0.19 | 105 | |
rs6056923 | 1.000 | 0.160 | 20 | 9840271 | intron variant | T/C | snv | 0.10 | 1 | ||
rs2157257 | 1.000 | 0.160 | 22 | 36312293 | intron variant | A/G | snv | 0.52 | 1 |