| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3828032 | 1.000 | 0.040 | 1 | 196951048 | intron variant | C/G;T | snv | 0.28 | 1 | ||
| rs9427934 | 1.000 | 0.040 | 1 | 196953730 | intron variant | G/A | snv | 0.32 | 1 | ||
| rs1853881 | 1.000 | 0.040 | 1 | 196946615 | intron variant | A/C | snv | 0.11 | 1 | ||
| rs432366 | 1.000 | 0.040 | 1 | 196943061 | upstream gene variant | C/G;T | snv | 1 | |||
| rs12066959 | 1 | 196948769 | intron variant | G/A | snv | 0.26 | 1 | ||||
| rs201886468 | 1 | 196948769 | intron variant | -/AT | delins | 1.4E-02 | 1 | ||||
| rs3790414 | 1 | 196951169 | intron variant | T/A | snv | 0.26 | 1 | ||||
| rs4085749 | 1 | 196951018 | stop gained | C/A;T | snv | 0.31 | 1 |