| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs41270082 | 1.000 | 0.080 | 6 | 35795160 | missense variant | G/A;C;T | snv | 8.5E-03; 4.0E-06 | 1 | ||
| rs3748051 | 1.000 | 0.080 | 6 | 35797166 | intron variant | T/C | snv | 0.23 | 0.22 | 1 | |
| rs3748050 | 1.000 | 0.080 | 6 | 35797291 | splice donor variant | T/C | snv | 0.25 | 0.26 | 1 |