Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7789162 | 7 | 44833301 | intron variant | T/C | snv | 0.48 | 3 | ||||
rs12155039 | 7 | 44833526 | intron variant | C/A;T | snv | 2 | |||||
rs12155038 | 7 | 44833378 | intron variant | G/A | snv | 0.40 | 1 | ||||
rs10267576 | 7 | 44831334 | intron variant | T/C | snv | 0.35 | 1 |