Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267606621 | 0.882 | 0.080 | 16 | 70268356 | missense variant | C/T | snv | 3 | |||
rs797044801 | 1.000 | 0.080 | 16 | 70254688 | missense variant | T/G | snv | 1 |