Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs752603642 | 0.925 | 0.160 | 16 | 2072888 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs137854052 | 1.000 | 0.120 | 16 | 2058765 | frameshift variant | -/C | delins | 1 | |||
| rs137854106 | 1.000 | 0.120 | 16 | 2079357 | frameshift variant | A/- | delins | 1 | |||
| rs137854329 | 1.000 | 0.120 | 16 | 2085238 | frameshift variant | -/T | delins | 1 | |||
| rs1459518095 | 1.000 | 0.120 | 16 | 2084552 | missense variant | C/G;T | snv | 4.2E-06 | 1 | ||
| rs397515225 | 1.000 | 0.120 | 16 | 2080366 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs45460895 | 1.000 | 0.120 | 16 | 2055520 | splice donor variant | G/A | snv | 1 | |||
| rs45488500 | 1.000 | 0.120 | 16 | 2054441 | splice donor variant | G/T | snv | 1 | |||
| rs45509500 | 1.000 | 0.120 | 16 | 2072923 | synonymous variant | C/G;T | snv | 4.0E-06; 5.6E-05 | 1 | ||
| rs45517115 | 1.000 | 0.120 | 16 | 2055518 | stop gained | C/T | snv | 1 | |||
| rs45517201 | 1.000 | 0.120 | 16 | 2070531 | missense variant | T/C | snv | 1 | |||
| rs45517278 | 1.000 | 0.120 | 16 | 2079090 | missense variant | G/T | snv | 1 | |||
| rs754504918 | 1.000 | 0.120 | 16 | 2071816 | missense variant | G/A | snv | 1 | |||
| rs764288120 | 1.000 | 0.120 | 16 | 2061983 | missense variant | T/C | snv | 4.0E-06 | 1 |