Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1351164 | 2 | 217407175 | intron variant | T/C | snv | 0.24 | 1 | ||||
rs6435999 | 2 | 217658439 | intron variant | A/G | snv | 0.12 | 1 | ||||
rs16857609 | 0.925 | 0.080 | 2 | 217431785 | intron variant | C/T | snv | 0.28 | 1 | ||
rs6759952 | 1.000 | 0.080 | 2 | 217406996 | intron variant | T/A;C | snv | 1 | |||
rs966423 | 0.776 | 0.200 | 2 | 217445617 | intron variant | C/G;T | snv | 1 |