Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1012657750 | 1 | 151368294 | missense variant | G/C | snv | 2 | |||||
rs1249051329 | 1 | 151369834 | synonymous variant | T/C | snv | 3.5E-05 | 2 | ||||
rs771038258 | 1 | 151365837 | missense variant | A/G | snv | 8.0E-06 | 2.1E-05 | 2 | |||
rs1308703978 | 1 | 151365194 | missense variant | C/A;T | snv | 4.0E-06 | 1 |