Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs141014084 | 1.000 | 0.080 | 5 | 177430911 | missense variant | G/A | snv | 2.0E-05 | 2.1E-05 | 1 | |
rs118204455 | 1.000 | 0.080 | 5 | 177406019 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
rs865853663 | 1.000 | 0.080 | 5 | 177403878 | missense variant | C/T | snv | 1 | |||
rs118204456 | 0.851 | 0.200 | 5 | 177404231 | missense variant | G/C;T | snv | 4.3E-06 | 1 | ||
rs932430490 | 1.000 | 0.080 | 5 | 177403859 | missense variant | C/T | snv | 1 | |||
rs118204454 | 1.000 | 0.080 | 5 | 177403994 | missense variant | C/G;T | snv | 4.4E-06 | 1 |