Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908565 | 1.000 | 0.160 | 6 | 43614181 | missense variant | A/C | snv | 2.4E-05 | 1.4E-05 | 1 | |
rs199562456 | 1.000 | 0.160 | 6 | 43614489 | missense variant | A/G | snv | 1.6E-04 | 6.3E-05 | 1 | |
rs56307355 | 1.000 | 0.160 | 6 | 43614018 | missense variant | A/C;G | snv | 8.0E-06; 8.7E-04 | 1 | ||
rs1413703153 | 1.000 | 0.160 | 6 | 43603915 | missense variant | G/T | snv | 4.0E-06 | 1 | ||
rs756931657 | 1.000 | 0.160 | 6 | 43587277 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs758423288 | 1.000 | 0.160 | 6 | 43587331 | missense variant | G/A | snv | 4.4E-05 | 6.3E-05 | 1 |