| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1483186 | 0.925 | 0.040 | 3 | 53165064 | intron variant | C/G;T | snv | 2 | |||
| rs1398084548 | 1.000 | 0.040 | 3 | 53179612 | missense variant | A/G | snv | 1.4E-05 | 1 | ||
| rs151079563 | 3 | 53160305 | intron variant | T/C | snv | 9.4E-04 | 1 | ||||
| rs2306574 | 1.000 | 0.040 | 3 | 53188745 | synonymous variant | C/T | snv | 0.75 | 0.75 | 1 |