| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
| rs12163644 | 1.000 | 0.080 | 3 | 14343616 | downstream gene variant | G/A | snv | 8.7E-02 | 1 | ||
| rs7512080 | 1.000 | 0.080 | 1 | 162639948 | intron variant | A/G | snv | 4.6E-02 | 1 | ||
| rs35648237 | 1.000 | 0.080 | 18 | 13478722 | intron variant | A/G | snv | 8.8E-02 | 1 |