| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs191486604 | 1.000 | 0.040 | 6 | 161350208 | missense variant | C/T | snv | 6.0E-05 | 1.3E-04 | 1 | |
| rs397514694 | 1.000 | 0.040 | 6 | 161350205 | missense variant | C/A | snv | 1 | |||
| rs532703934 | 1.000 | 0.040 | 6 | 162443438 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs55774500 | 1.000 | 0.040 | 6 | 162262692 | missense variant | G/A;T | snv | 8.0E-06; 3.6E-03 | 1 | ||
| rs55830907 | 1.000 | 0.040 | 6 | 161360169 | missense variant | G/A | snv | 1.9E-03 | 1.9E-03 | 1 | |
| rs55961220 | 1.000 | 0.040 | 6 | 161785778 | missense variant | A/C | snv | 1 | |||
| rs566229879 | 1.000 | 0.040 | 6 | 162262662 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs754809877 | 1.000 | 0.040 | 6 | 162443326 | frameshift variant | T/- | delins | 3.1E-04 | 1 | ||
| rs763652747 | 1.000 | 0.040 | 6 | 161548996 | missense variant | C/T | snv | 2.8E-05 | 7.0E-06 | 1 | |
| rs778125254 | 1.000 | 0.040 | 6 | 161360129 | missense variant | G/T | snv | 8.0E-06 | 1 | ||
| rs778305273 | 1.000 | 0.040 | 6 | 161350176 | missense variant | A/G | snv | 5.2E-05 | 1 | ||
| rs9456735 | 1.000 | 0.040 | 6 | 162054135 | start lost | T/A;G | snv | 4.0E-06; 4.4E-03 | 1 |