| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs78378222 | 0.662 | 0.360 | 17 | 7668434 | 3 prime UTR variant | T/G | snv | 8.3E-03 | 37 | ||
| rs5742915 | 0.925 | 0.080 | 15 | 74044292 | missense variant | T/C;G | snv | 0.35; 4.0E-06 | 7 | ||
| rs7223535 | 1.000 | 0.080 | 17 | 30884649 | intron variant | G/A | snv | 0.25 | 4 | ||
| rs147110934 | 19 | 55482069 | missense variant | G/T | snv | 1.4E-02 | 1.5E-02 | 3 | |||
| rs34776209 | 7 | 23473474 | upstream gene variant | C/T | snv | 0.18 | 3 | ||||
| rs72656010 | 8 | 56209656 | intron variant | T/C | snv | 0.10 | 3 |