Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780641693 | 1.000 | 0.040 | 7 | 87462832 | missense variant | A/T | snv | 4.0E-06 | 1 | ||
rs8187797 | 1.000 | 0.040 | 7 | 87439814 | missense variant | C/G | snv | 2.1E-03 | 8.7E-03 | 1 | |
rs970324585 | 1.000 | 0.040 | 7 | 87423931 | missense variant | G/A | snv | 1 | |||
rs972726699 | 1.000 | 0.040 | 7 | 87426875 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 |