Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs56149945 | 0.595 | 0.680 | 5 | 143399752 | missense variant | T/A;C | snv | 2.0E-02 | 49 | ||
rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 58 | |
rs137853226 | 0.882 | 0.160 | 3 | 50256262 | missense variant | C/G;T | snv | 3 | |||
rs773454677 | 0.925 | 0.160 | 7 | 55205466 | missense variant | G/A | snv | 1.2E-05 | 3 | ||
rs672601307 | 1.000 | 0.080 | 15 | 50490443 | missense variant | T/C | snv | 2 | |||
rs672601306 | 1.000 | 0.080 | 15 | 50490442 | inframe deletion | TCC/- | delins | 1 | |||
rs672601308 | 1.000 | 0.080 | 15 | 50490444 | missense variant | C/G | snv | 1 | |||
rs672601311 | 1.000 | 0.080 | 15 | 50490450 | missense variant | C/G | snv | 1 |