| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3785356 | 0.925 | 0.080 | 16 | 27337847 | intron variant | C/T | snv | 0.25 | 5 | ||
| rs3024655 | 0.925 | 0.080 | 16 | 27358181 | intron variant | A/G;T | snv | 2 | |||
| rs1805013 | 0.925 | 0.120 | 16 | 27362659 | missense variant | C/T | snv | 3.6E-02 | 3.6E-02 | 1 | |
| rs145986476 | 1.000 | 0.080 | 16 | 27348194 | intron variant | C/A | snv | 5.3E-03 | 1 | ||
| rs3024622 | 1.000 | 0.080 | 16 | 27354132 | non coding transcript exon variant | C/A;G;T | snv | 1 | |||
| rs3024665 | 1.000 | 0.040 | 16 | 27360218 | intron variant | C/T | snv | 0.80 | 1 | ||
| rs2072130 | 16 | 27345077 | non coding transcript exon variant | C/G;T | snv | 1 |