Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10079250 | 0.827 | 0.120 | 5 | 150070569 | missense variant | T/C | snv | 9.9E-02 | 8.6E-02 | 7 | |
rs121913390 | 5 | 150073481 | stop gained | A/G;T | snv | 2 | |||||
rs121913393 | 5 | 150054083 | missense variant | A/G | snv | 2 | |||||
rs1801271 | 5 | 150054082 | missense variant | T/A;C | snv | 2 | |||||
rs121913392 | 5 | 150054081 | stop gained | A/C;T | snv | 1 |