Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7137828 | 0.763 | 0.200 | 12 | 111494996 | intron variant | C/A;T | snv | 14 | |||
rs604723 | 1.000 | 0.040 | 11 | 100739815 | intron variant | T/C | snv | 0.78 | 8 | ||
rs13139571 | 1.000 | 0.040 | 4 | 155724361 | intron variant | C/A | snv | 0.22 | 7 | ||
rs7209400 | 1.000 | 0.040 | 17 | 49372695 | intron variant | C/T | snv | 0.47 | 6 |