Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387906597 | 0.851 | 0.280 | 14 | 53950667 | stop gained | G/A;C | snv | 8.0E-06 | 4 | ||
rs121912767 | 1.000 | 0.120 | 14 | 53951951 | missense variant | G/C | snv | 1.8E-04 | 1.7E-04 | 1 | |
rs770493925 | 1.000 | 0.120 | 14 | 53950774 | missense variant | C/T | snv | 1.8E-04 | 4.2E-05 | 1 | |
rs121912766 | 1.000 | 0.120 | 14 | 53950222 | missense variant | G/A | snv | 1 | |||
rs121912768 | 1.000 | 0.120 | 14 | 53950399 | missense variant | C/A;T | snv | 8.2E-04 | 1 |