Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs419137 | 1 | 196727745 | intron variant | G/T | snv | 0.92 | 1 | ||||
rs10494745 | 1.000 | 0.040 | 1 | 196918327 | missense variant | G/A | snv | 8.0E-02 | 7.4E-02 | 1 | |
rs10801582 | 1 | 196975227 | upstream gene variant | G/A | snv | 0.22 | 1 | ||||
rs2786107 | 1 | 197341647 | intron variant | G/T | snv | 0.80 | 1 | ||||
rs10754218 | 1 | 197195884 | intron variant | G/A | snv | 0.60 | 1 |