Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs375129902 | 0.882 | 0.080 | 6 | 6151852 | missense variant | T/C | snv | 7.2E-05 | 5.6E-05 | 3 | |
rs369187276 | 0.882 | 0.080 | 6 | 6167531 | missense variant | C/G;T | snv | 4.0E-06; 9.1E-05 | 3 | ||
rs1173258177 | 1.000 | 0.080 | 6 | 6151855 | missense variant | A/G | snv | 1 | |||
rs1561673120 | 1.000 | 0.080 | 6 | 6266566 | missense variant | C/A | snv | 1 |