Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4608502 | 2 | 227269439 | intron variant | T/A;C | snv | 3 | |||||
rs11553764 | 12 | 104021466 | 5 prime UTR variant | C/T | snv | 0.13 | 2 | ||||
rs28687756 | 16 | 88295322 | intron variant | T/G | snv | 6.5E-04 | 2 | ||||
rs3118515 | 9 | 134544468 | intron variant | G/A;C;T | snv | 2 | |||||
rs56009602 | 11 | 130419717 | intron variant | C/A;T | snv | 2 |