| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800947 | 0.683 | 0.440 | 1 | 159713648 | splice region variant | C/A;G;T | snv | 4.4E-05; 5.1E-02; 4.0E-06 | 28 | ||
| rs14259 | 0.724 | 0.360 | 12 | 121915890 | missense variant | A/C;G | snv | 4.0E-06; 0.32 | 19 | ||
| rs765798193 | 0.732 | 0.320 | 12 | 121915884 | frameshift variant | G/-;GG | delins | 18 | |||
| rs4580704 | 0.790 | 0.200 | 4 | 55460540 | intron variant | G/C | snv | 0.69 | 13 | ||
| rs2072446 | 0.776 | 0.160 | 17 | 49510457 | missense variant | C/T | snv | 5.2E-02 | 4.1E-02 | 11 | |
| rs10988134 | 0.925 | 0.080 | 9 | 128833128 | 3 prime UTR variant | C/T | snv | 0.34 | 4 | ||
| rs1187323 | 0.882 | 0.080 | 9 | 84668501 | upstream gene variant | C/A;G;T | snv | 5 |