Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1390938 | 0.807 | 0.200 | 8 | 20179202 | missense variant | A/G | snv | 0.71 | 0.78 | 7 | |
rs12938031 | 0.851 | 0.160 | 17 | 45777136 | intron variant | A/G | snv | 0.26 | 6 | ||
rs7209436 | 0.851 | 0.200 | 17 | 45792776 | intron variant | C/T | snv | 0.43 | 5 | ||
rs8067056 | 0.925 | 0.080 | 17 | 46006582 | intron variant | T/C;G | snv | 0.30 | 5 | ||
rs62081501 | 0.925 | 0.080 | 18 | 37627749 | intron variant | G/A | snv | 6.2E-02 | 4 | ||
rs483143 | 0.925 | 0.080 | 6 | 27878966 | intergenic variant | G/C | snv | 0.13 | 2 | ||
rs7867155 | 0.925 | 0.080 | 9 | 96065532 | intron variant | C/T | snv | 0.13 | 2 | ||
rs9980603 | 0.925 | 0.080 | 21 | 40514656 | intron variant | T/C | snv | 0.40 | 2 |