Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35808169 | 0.776 | 0.080 | 12 | 4259441 | intron variant | T/C | snv | 0.17 | 10 | ||
rs10774214 | 0.790 | 0.080 | 12 | 4259186 | intron variant | T/C | snv | 0.54 | 9 | ||
rs4572213 | 0.790 | 0.080 | 12 | 4256383 | intron variant | A/T | snv | 0.10 | 9 | ||
rs12818766 | 0.790 | 0.080 | 12 | 4266925 | intron variant | G/A | snv | 0.17 | 9 | ||
rs76895963 | 1.000 | 0.080 | 12 | 4275678 | intron variant | T/G | snv | 1.5E-02 | 6 | ||
rs71061176 | 12 | 4269579 | intron variant | -/T | ins | 0.18 | 1 | ||||
rs11063069 | 0.925 | 0.080 | 12 | 4265207 | intron variant | A/G | snv | 0.20 | 1 |