Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11209718 | 1 | 41223266 | intron variant | C/G;T | snv | 2 | |||||
rs6686842 | 1 | 41065199 | intron variant | T/C | snv | 0.65 | 2 | ||||
rs114233776 | 1 | 41152625 | missense variant | G/A | snv | 4.7E-03 | 4.7E-03 | 1 | |||
rs6600365 | 1 | 41090581 | intron variant | C/T | snv | 0.65 | 1 |