Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3730358 | 0.724 | 0.360 | 14 | 104780070 | intron variant | G/A;C | snv | 0.16; 4.0E-03 | 14 | ||
rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 54 | ||
rs2494752 | 0.790 | 0.120 | 14 | 104797271 | upstream gene variant | A/G | snv | 0.85 | 10 | ||
rs3803304 | 0.882 | 0.160 | 14 | 104772809 | intron variant | C/G | snv | 0.24 | 3 | ||
rs2494740 | 0.925 | 0.080 | 14 | 104781544 | intron variant | A/T | snv | 0.61 | 2 | ||
rs2494744 | 0.925 | 0.080 | 14 | 104789477 | intron variant | A/G | snv | 0.83 | 2 | ||
rs2498789 | 0.925 | 0.080 | 14 | 104783708 | intron variant | A/G | snv | 0.26 | 2 |