Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4775301 | 0.925 | 0.040 | 15 | 60834660 | intron variant | T/C;G | snv | 2 | |||
rs8024133 | 0.925 | 0.040 | 15 | 60838440 | intron variant | C/T | snv | 0.42 | 2 | ||
rs8041061 | 0.925 | 0.040 | 15 | 60832639 | intron variant | G/T | snv | 0.39 | 2 | ||
rs8042149 | 0.882 | 0.160 | 15 | 60832754 | intron variant | T/G | snv | 0.44 | 2 |