| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3025000 | 1.000 | 0.120 | 6 | 43778432 | non coding transcript exon variant | C/T | snv | 0.29 | 0.23 | 1 | |
| rs3025010 | 6 | 43779840 | non coding transcript exon variant | T/C;G | snv | 1 | |||||
| rs3025036 | 1.000 | 0.080 | 6 | 43783932 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
| rs376388064 | 6 | 43782006 | missense variant | C/T | snv | 2.8E-05 | 3.5E-05 | 1 | |||
| rs541717889 | 6 | 43770888 | missense variant | G/C | snv | 2.1E-05 | 1 | ||||
| rs554561071 | 6 | 43777513 | missense variant | A/G | snv | 1.2E-05 | 3.5E-05 | 1 | |||
| rs735286 | 6 | 43776884 | non coding transcript exon variant | C/T | snv | 0.23 | 1 | ||||
| rs749491856 | 1.000 | 6 | 43782071 | missense variant | A/C | snv | 1 | ||||
| rs774265827 | 6 | 43780773 | missense variant | G/A;T | snv | 8.0E-06; 2.0E-05 | 1 |