Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7330914 | 13 | 110274714 | intron variant | C/A | snv | 3.0E-02 | 3 | ||||
rs7998875 | 13 | 110289053 | intron variant | G/A;T | snv | 3 | |||||
rs4773144 | 0.827 | 0.080 | 13 | 110308365 | intron variant | A/G | snv | 0.42 | 3 | ||
rs3809346 | 1.000 | 0.080 | 13 | 110308596 | intron variant | G/A;C | snv | 2 | |||
rs494558 | 13 | 110276815 | intron variant | C/T | snv | 0.90 | 1 | ||||
rs3742207 | 0.925 | 0.120 | 13 | 110166251 | missense variant | T/A;G | snv | 2.8E-05; 0.30 | 1 | ||
rs11617955 | 1.000 | 0.040 | 13 | 110165755 | intron variant | T/A | snv | 9.3E-02 | 1 | ||
rs12873154 | 1.000 | 0.040 | 13 | 110268505 | intron variant | A/G | snv | 8.7E-02 | 1 |