Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387907152 | 0.925 | 0.160 | 19 | 55165427 | stop gained | G/A | snv | 7.0E-06 | 3 | ||
rs387907151 | 0.925 | 0.160 | 19 | 55165904 | missense variant | A/G | snv | 2 | |||
rs770403610 | 1.000 | 0.160 | 19 | 55162263 | stop gained | C/T | snv | 2.1E-05 | 2 | ||
rs397515395 | 0.925 | 0.160 | 19 | 55161684 | frameshift variant | -/A | delins | 7.3E-06; 7.3E-06 | 2 | ||
rs1349668884 | 1.000 | 0.160 | 19 | 55159416 | frameshift variant | -/T | delins | 2 |