Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267607144 | 0.716 | 0.360 | 12 | 109800665 | missense variant | C/T | snv | 17 | |||
rs387907219 | 1.000 | 0.080 | 12 | 109800659 | missense variant | C/G;T | snv | 1.6E-05 | 1 | ||
rs387907220 | 1.000 | 0.080 | 12 | 109800662 | missense variant | C/A | snv | 1 | |||
rs515726170 | 1.000 | 0.080 | 12 | 109800652 | missense variant | G/C | snv | 1 |