Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5743289 | 1.000 | 0.040 | 16 | 50722863 | intron variant | C/G;T | snv | 2 | |||
rs17221417 | 0.925 | 0.040 | 16 | 50705671 | intron variant | C/G | snv | 0.20 | 1 | ||
rs2076756 | 0.882 | 0.040 | 16 | 50722970 | intron variant | A/G | snv | 0.17 | 2 | ||
rs5743293 | 0.807 | 0.200 | 16 | 50729868 | frameshift variant | C/-;CC | delins | 5 | |||
rs2066845 | 0.611 | 0.600 | 16 | 50722629 | missense variant | G/C;T | snv | 1.1E-02; 2.2E-04 | 5 | ||
rs2066844 | 0.587 | 0.520 | 16 | 50712015 | missense variant | C/T | snv | 2.6E-02 | 2.9E-02 | 5 |