Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104895097 | 0.925 | 0.040 | 16 | 3243205 | missense variant | C/T | snv | 2.0E-04 | 1.1E-04 | 2 | |
rs61732874 | 0.925 | 0.040 | 16 | 3243257 | missense variant | C/A;T | snv | 1.8E-03; 1.2E-05 | 2 | ||
rs28940579 | 0.732 | 0.440 | 16 | 3243310 | missense variant | A/G;T | snv | 2.2E-03; 4.0E-06 | 13 | ||
rs104895091 | 0.925 | 0.040 | 16 | 3243404 | inframe deletion | CAT/- | delins | 2 | |||
rs28940578 | 0.716 | 0.400 | 16 | 3243405 | missense variant | C/T | snv | 1.4E-04 | 6.3E-05 | 16 | |
rs61752717 | 0.583 | 0.840 | 16 | 3243407 | missense variant | T/A;C | snv | 2.8E-04 | 72 | ||
rs28940580 | 0.742 | 0.560 | 16 | 3243447 | missense variant | C/A;G;T | snv | 1.0E-04; 8.0E-06 | 17 | ||
rs104895128 | 0.882 | 0.160 | 16 | 3243593 | missense variant | C/A;T | snv | 3.7E-05 | 3 | ||
rs104895105 | 0.851 | 0.120 | 16 | 3247171 | missense variant | G/A | snv | 7 |