Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267607490 | 0.925 | 0.160 | 2 | 219425734 | missense variant | C/T | snv | 4 | |||
rs150974575 | 1.000 | 0.160 | 2 | 219423817 | stop gained | C/T | snv | 1.2E-05 | 3 | ||
rs267607483 | 1.000 | 0.160 | 2 | 219420349 | splice region variant | A/G;T | snv | 2 | |||
rs267607495 | 2 | 219418497 | missense variant | C/T | snv | 2 | |||||
rs62636495 | 0.925 | 0.200 | 2 | 219418500 | missense variant | C/A;T | snv | 2 | |||
rs397516695 | 0.882 | 0.040 | 2 | 219418869 | missense variant | T/A;C | snv | 5.5E-05 | 1 | ||
rs727504448 | 2 | 219420116 | frameshift variant | G/- | del | 7.0E-06 | 2 |