Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs58072617 | 0.790 | 0.120 | 12 | 52517702 | missense variant | A/G;T | snv | 7 | |||
rs59115483 | 0.882 | 0.080 | 12 | 52519789 | missense variant | C/T | snv | 2.4E-05 | 7.0E-06 | 4 | |
rs59190510 | 0.851 | 0.080 | 12 | 52516647 | stop gained | C/A;T | snv | 4 | |||
rs762236241 | 0.882 | 0.080 | 17 | 75757312 | splice donor variant | T/C | snv | 2.0E-05 | 3 | ||
rs58762773 | 0.882 | 0.080 | 17 | 41583245 | missense variant | C/G;T | snv | 4.0E-06 | 3 | ||
rs59966597 | 1.000 | 0.080 | 17 | 41583347 | missense variant | G/A;C | snv | 4.0E-06 | 3 | ||
rs61027685 | 0.882 | 0.080 | 17 | 41586438 | missense variant | C/A;G;T | snv | 3 | |||
rs60586163 | 0.882 | 0.080 | 12 | 52519137 | missense variant | G/A;C;T | snv | 4.0E-06 | 3 | ||
rs57358989 | 0.925 | 0.080 | 17 | 41586478 | missense variant | C/T | snv | 2 | |||
rs61263401 | 0.925 | 0.080 | 17 | 41586480 | missense variant | T/C | snv | 2 | |||
rs57142010 | 0.925 | 0.080 | 12 | 52517699 | missense variant | T/A;C | snv | 2 | |||
rs58766676 | 0.925 | 0.080 | 12 | 52519120 | missense variant | T/A;C;G | snv | 2 | |||
rs59464425 | 0.925 | 0.080 | 12 | 52517698 | missense variant | G/A;T | snv | 2 | |||
rs61222761 | 0.925 | 0.080 | 12 | 52519824 | missense variant | T/A | snv | 2 | |||
rs61495052 | 0.925 | 0.080 | 12 | 52519767 | missense variant | T/C | snv | 2 | |||
rs56974573 | 1.000 | 0.080 | 17 | 41583384 | inframe deletion | CCT/- | delins | 1 | |||
rs57200223 | 1.000 | 0.080 | 17 | 41583287 | missense variant | G/A;T | snv | 1.6E-05 | 1 | ||
rs58378809 | 1.000 | 0.080 | 17 | 41586393 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs58560979 | 1.000 | 0.080 | 17 | 41583879 | missense variant | C/T | snv | 1 | |||
rs58645163 | 1.000 | 0.080 | 17 | 41583346 | missense variant | C/G;T | snv | 1.5E-04 | 1 | ||
rs58785777 | 1.000 | 0.080 | 17 | 41583866 | missense variant | G/T | snv | 1 | |||
rs59271739 | 1.000 | 0.080 | 17 | 41586487 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
rs59375065 | 1.000 | 0.080 | 17 | 41583869 | missense variant | T/C | snv | 1 | |||
rs59442925 | 1.000 | 0.080 | 17 | 41583265 | missense variant | T/C | snv | 1 | |||
rs60589227 | 1.000 | 0.080 | 17 | 41584390 | missense variant | C/A;G;T | snv | 3.2E-05; 1.6E-05 | 1 |