Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2302427 | 1.000 | 0.080 | 7 | 148828812 | missense variant | C/G | snv | 7.8E-02 | 6.0E-02 | 4 | |
rs267601395 | 0.925 | 0.160 | 7 | 148811636 | missense variant | A/G;T | snv | 7 | |||
rs3757441 | 0.752 | 0.200 | 7 | 148827660 | intron variant | C/T | snv | 0.80 | 12 | ||
rs41277434 | 0.851 | 0.160 | 7 | 148809304 | splice region variant | A/C;G | snv | 6.8E-02; 8.0E-06 | 6 | ||
rs887569 | 0.882 | 0.120 | 7 | 148808210 | intron variant | C/T | snv | 0.73 | 5 |