Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs8056611 | 1.000 | 0.040 | 16 | 50733736 | 3 prime UTR variant | A/G | snv | 0.56 | 1 | ||
rs2066842 | 0.763 | 0.200 | 16 | 50710713 | missense variant | C/A;T | snv | 4.0E-06; 0.19 | 1 | ||
rs749910 | 1.000 | 0.040 | 16 | 50724938 | intron variant | G/A | snv | 0.17 | 1 | ||
rs751271 | 1.000 | 0.040 | 16 | 50717264 | intron variant | T/G | snv | 0.61 | 1 | ||
rs17313265 | 1.000 | 0.040 | 16 | 50713793 | intron variant | C/T | snv | 0.20 | 1 | ||
rs8057341 | 0.925 | 0.080 | 16 | 50704069 | intron variant | A/G | snv | 0.68 | 1 | ||
rs17312836 | 1.000 | 0.040 | 16 | 50707551 | intron variant | A/C | snv | 0.33 | 1 | ||
rs2066844 | 0.587 | 0.520 | 16 | 50712015 | missense variant | C/T | snv | 2.6E-02 | 2.9E-02 | 1 | |
rs2066845 | 0.611 | 0.600 | 16 | 50722629 | missense variant | G/C;T | snv | 1.1E-02; 2.2E-04 | 1 | ||
rs3135499 | 0.882 | 0.160 | 16 | 50732216 | splice donor variant | A/C | snv | 0.45 | 1 | ||
rs17221417 | 0.925 | 0.040 | 16 | 50705671 | intron variant | C/G | snv | 0.20 | 1 | ||
rs2076753 | 1.000 | 0.040 | 16 | 50699463 | intron variant | G/A;T | snv | 0.20 | 1 | ||
rs5743291 | 0.925 | 0.040 | 16 | 50723365 | missense variant | G/A | snv | 6.3E-02 | 6.0E-02 | 1 | |
rs2066843 | 0.925 | 0.040 | 16 | 50711288 | synonymous variant | C/A;T | snv | 0.19 | 1 | ||
rs2066847 | 0.716 | 0.400 | 16 | 50729868 | frameshift variant | C/-;CC | delins | 1.5E-02 | 2 | ||
rs199883290 | 0.925 | 0.120 | 16 | 50729867 | missense variant | G/A;C | snv | 4.0E-06; 1.5E-02 | 7.0E-06 | 2 | |
rs540973741 | 0.925 | 0.120 | 16 | 50729868 | frameshift variant | C/-;CC | delins | 2 | |||
rs5743293 | 0.807 | 0.200 | 16 | 50729868 | frameshift variant | C/-;CC | delins | 2 | |||
rs2076756 | 0.882 | 0.040 | 16 | 50722970 | intron variant | A/G | snv | 0.17 | 2 | ||
rs5743289 | 1.000 | 0.040 | 16 | 50722863 | intron variant | C/G;T | snv | 2 |