Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6235 | 0.925 | 0.120 | 5 | 96393194 | missense variant | C/G | snv | 0.26 | 0.23 | 8 | |
rs6234 | 0.851 | 0.160 | 5 | 96393270 | missense variant | G/C | snv | 0.27 | 0.24 | 8 | |
rs6232 | 0.925 | 0.080 | 5 | 96416081 | missense variant | T/C | snv | 3.9E-02 | 3.2E-02 | 2 | |
rs750845408 | 0.925 | 0.080 | 5 | 96423317 | missense variant | T/C | snv | 4.5E-05 | 7.0E-05 | 2 | |
rs155971 | 1.000 | 0.080 | 5 | 96414692 | intron variant | T/C | snv | 0.57 | 1 | ||
rs765019354 | 1.000 | 0.080 | 5 | 96429260 | stop gained | G/A;C | snv | 4.0E-06; 1.6E-05 | 1 |