Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs140365820 | 0.925 | 0.160 | 9 | 12704706 | splice donor variant | G/A | snv | 5.6E-05 | 2.0E-04 | 2 | |
rs281865424 | 0.925 | 0.160 | 9 | 12702424 | missense variant | G/A;T | snv | 2.8E-05 | 2 | ||
rs387906562 | 1.000 | 0.160 | 9 | 12702411 | frameshift variant | AACA/- | delins | 1 | |||
rs104894130 | 0.925 | 0.160 | 9 | 12695626 | stop gained | C/G | snv | 6.0E-05 | 2.1E-04 | 3 | |
rs387906561 | 1.000 | 0.160 | 9 | 12694101 | frameshift variant | T/- | delins | 1 | |||
rs61758405 | 1.000 | 0.160 | 9 | 12694066 | missense variant | G/A | snv | 1.9E-03 | 1.7E-03 | 1 | |
rs387906560 | 0.925 | 0.160 | 9 | 12704545 | frameshift variant | A/- | delins | 2 | |||
rs121912778 | 1.000 | 0.160 | 9 | 12704564 | stop gained | C/T | snv | 2.8E-05 | 6.3E-05 | 1 | |
rs776174514 | 1.000 | 0.160 | 9 | 12704589 | missense variant | T/C | snv | 4.0E-06 | 1 |