| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2321168 | 13 | 33279354 | non coding transcript exon variant | G/A | snv | 0.98 | 4 | ||||
| rs2555592 | 13 | 33202766 | intron variant | T/G | snv | 4.3E-02 | 2 | ||||
| rs2764627 | 0.925 | 0.040 | 13 | 33202941 | intron variant | C/T | snv | 5.0E-02 | 2 | ||
| rs9315204 | 1.000 | 0.080 | 13 | 33119700 | intron variant | C/T | snv | 0.20 | 1 | ||
| rs1980781 | 1.000 | 0.080 | 13 | 33126237 | synonymous variant | T/A;G | snv | 8.0E-06; 0.25 | 1 | ||
| rs3742321 | 1.000 | 0.080 | 13 | 33129928 | missense variant | T/C | snv | 0.24 | 0.20 | 1 | |
| rs6561821 | 13 | 33287048 | intron variant | A/T | snv | 0.97 | 1 |