Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs756465037 | 0.807 | 0.200 | 3 | 46439392 | missense variant | C/G | snv | 8.0E-06 | 7.0E-06 | 6 | |
rs104895224 | 0.882 | 0.080 | 12 | 6333808 | missense variant | C/G;T | snv | 3 | |||
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
rs28940578 | 0.716 | 0.400 | 16 | 3243405 | missense variant | C/T | snv | 1.4E-04 | 6.3E-05 | 16 | |
rs224222 | 0.724 | 0.440 | 16 | 3254463 | missense variant | C/T | snv | 0.24 | 0.21 | 15 | |
rs104895218 | 0.827 | 0.240 | 12 | 6334099 | missense variant | C/T | snv | 5 | |||
rs5743708 | 0.525 | 0.800 | 4 | 153705165 | missense variant | G/A | snv | 1.7E-02 | 1.8E-02 | 98 | |
rs104895105 | 0.851 | 0.120 | 16 | 3247171 | missense variant | G/A | snv | 7 | |||
rs61752717 | 0.583 | 0.840 | 16 | 3243407 | missense variant | T/A;C | snv | 2.8E-04 | 72 |