| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10793565 | 10 | 44892783 | intron variant | G/C | snv | 0.53 | 2 | ||||
| rs10736831 | 10 | 44906863 | intron variant | G/A | snv | 0.55 | 2 | ||||
| rs2281841 | 10 | 44911160 | intron variant | T/C | snv | 0.53 | 2 | ||||
| rs7099692 | 10 | 44896515 | intron variant | G/A;C | snv | 1 | |||||
| rs397731217 | 10 | 44904499 | intron variant | A/-;AA;AAA;AAAA;AAAAA | delins | 1 | |||||
| rs7909074 | 10 | 44900391 | non coding transcript exon variant | G/A | snv | 0.53 | 1 | ||||
| rs4948643 | 10 | 44884311 | intron variant | T/C | snv | 0.65 | 1 |