Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1254203917 | 1.000 | 0.160 | X | 67721881 | missense variant | G/T | snv | 5.5E-06 | 1 | ||
| rs1355285524 | 1.000 | 0.160 | X | 67546480 | missense variant | A/G | snv | 1.8E-05 | 1.0E-05 | 1 | |
| rs137852563 | 1.000 | 0.160 | X | 67711673 | stop gained | G/A | snv | 5.7E-06 | 1 | ||
| rs137852566 | 1.000 | 0.160 | X | 67686012 | stop gained | A/T | snv | 1 | |||
| rs137852568 | 1.000 | 0.160 | X | 67723728 | stop gained | A/T | snv | 1 | |||
| rs137852570 | 1.000 | 0.160 | X | 67721876 | missense variant | A/G | snv | 1 | |||
| rs137852575 | 1.000 | 0.160 | X | 67545324 | stop gained | C/T | snv | 1 | |||
| rs137852579 | 1.000 | 0.160 | X | 67711549 | missense variant | T/C | snv | 1 | |||
| rs137852585 | 1.000 | 0.160 | X | 67711639 | missense variant | T/G | snv | 1 | |||
| rs137852586 | 1.000 | 0.160 | X | 67643378 | missense variant | G/A;T | snv | 1 | |||
| rs137852594 | 1.000 | 0.160 | X | 67723745 | synonymous variant | C/T | snv | 1 | |||
| rs137852596 | 1.000 | 0.160 | X | 67643371 | missense variant | G/A | snv | 1 | |||
| rs137852597 | 1.000 | 0.160 | X | 67722973 | missense variant | T/C | snv | 1 | |||
| rs137852598 | 1.000 | 0.160 | X | 67722948 | missense variant | C/G;T | snv | 5.5E-06 | 1 | ||
| rs137852599 | 1.000 | 0.160 | X | 67711585 | missense variant | A/C | snv | 1 | |||
| rs1481151440 | 1.000 | 0.160 | X | 67545467 | stop gained | C/A;T | snv | 1 | |||
| rs1555969512 | 1.000 | 0.160 | X | 67545360 | stop gained | C/T | snv | 1 | |||
| rs1555969545 | 1.000 | 0.160 | X | 67545414 | stop gained | C/T | snv | 1 | |||
| rs1555969682 | 1.000 | 0.160 | X | 67545889 | missense variant | G/T | snv | 1 | |||
| rs1555969694 | 1.000 | 0.160 | X | 67545936 | frameshift variant | -/G | delins | 1 | |||
| rs1555969807 | 1.000 | 0.160 | X | 67546331 | stop gained | C/A | snv | 1 | |||
| rs1555982860 | 1.000 | 0.160 | X | 67643327 | missense variant | G/A | snv | 1 | |||
| rs1555990485 | 1.000 | 0.160 | X | 67686087 | missense variant | C/T | snv | 1 | |||
| rs1555990488 | 1.000 | 0.160 | X | 67686091 | missense variant | T/C | snv | 1 | |||
| rs1555995750 | 1.000 | 0.160 | X | 67711402 | frameshift variant | C/- | delins | 1 |