| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs45483392 | 0.925 | 0.120 | 16 | 2087897 | missense variant | C/A;T | snv | 2 | |||
| rs45487497 | 0.925 | 0.120 | 16 | 2058779 | missense variant | G/A | snv | 2 | |||
| rs45516293 | 0.925 | 0.120 | 16 | 2084965 | missense variant | A/C;G | snv | 2 | |||
| rs45517169 | 0.925 | 0.120 | 16 | 2062982 | stop gained | C/T | snv | 2 | |||
| rs45517258 | 0.925 | 0.120 | 16 | 2076141 | missense variant | C/G;T | snv | 2 | |||
| rs45517308 | 0.925 | 0.120 | 16 | 2081734 | stop gained | C/A;G;T | snv | 8.0E-06 | 2 | ||
| rs45517382 | 0.925 | 0.120 | 16 | 2086834 | missense variant | A/G | snv | 2 | |||
| rs1174984399 | 1.000 | 0.120 | 3 | 138714505 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| 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 | |||
| rs138742347 | 1.000 | 0.120 | 1 | 9722244 | splice region variant | C/T | snv | 5.8E-04 | 2.5E-03 | 1 | |
| rs1430119276 | 1.000 | 0.120 | 16 | 2079096 | missense variant | G/T | snv | 7.0E-06 | 1 | ||
| rs1459518095 | 1.000 | 0.120 | 16 | 2084552 | missense variant | C/G;T | snv | 4.2E-06 | 1 | ||
| rs148838884 | 1.000 | 0.120 | 1 | 9722067 | synonymous variant | C/T | snv | 4.4E-05 | 5.6E-05 | 1 | |
| rs1554815914 | 1.000 | 0.120 | 9 | 132905874 | frameshift variant | TCCCGCA/GC | delins | 1 | |||
| rs185159716 | 1.000 | 0.120 | 9 | 132906751 | missense variant | A/G | snv | 4.0E-06 | 7.0E-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 | |||
| rs45517423 | 1.000 | 0.120 | 16 | 2088569 | missense variant | C/T | snv | 1.5E-03 | 1.5E-03 | 1 |