Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs73885319 | 0.851 | 0.120 | 22 | 36265860 | missense variant | A/G | snv | 1.6E-02 | 6.6E-02 | 6 | |
rs60910145 | 0.851 | 0.120 | 22 | 36265988 | missense variant | T/G | snv | 1.6E-02 | 6.6E-02 | 5 | |
rs71785313 | 0.882 | 0.120 | 22 | 36265996 | inframe deletion | TTATAA/- | delins | 5 | |||
rs1428826948 | 0.925 | 0.040 | 22 | 36265940 | synonymous variant | T/G | snv | 1.2E-05 | 3 | ||
rs1569534160 | 0.925 | 0.040 | 22 | 36265812 | missense variant | A/G | snv | 3 |