Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 8 | ||
rs3197999 | 0.732 | 0.280 | 3 | 49684099 | missense variant | G/A | snv | 0.26 | 0.27 | 6 | |
rs917997 | 0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv | 6 | |||
rs10758669 | 0.763 | 0.280 | 9 | 4981602 | upstream gene variant | C/A;T | snv | 5 | |||
rs2188962 | 0.882 | 0.160 | 5 | 132435113 | intron variant | C/T | snv | 0.29 | 4 | ||
rs1847472 | 0.807 | 0.200 | 6 | 90263440 | intron variant | C/A | snv | 0.25 | 3 | ||
rs8005161 | 0.882 | 0.120 | 14 | 88006251 | intron variant | C/T | snv | 0.18 | 3 |