Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11734460 | 4 | 711285 | intron variant | C/A;T | snv | 4 | |||||
rs79839061 | 4 | 712095 | intron variant | G/A | snv | 9.6E-02 | 1 | ||||
rs56011263 | 4 | 709183 | intron variant | T/C | snv | 0.35 | 1 | ||||
rs75751670 | 4 | 707252 | intron variant | G/A | snv | 0.10 | 1 | ||||
rs79713586 | 4 | 735866 | intron variant | A/T | snv | 6.4E-02 | 1 | ||||
rs142708984 | 4 | 707538 | intron variant | C/A;T | snv | 1 |