Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
rs5516 | 0.827 | 0.120 | 19 | 50820217 | missense variant | C/G | snv | 0.69 | 0.67 | 6 | |
rs140598 | 0.827 | 0.160 | 15 | 48487333 | missense variant | G/A;C | snv | 3.2E-02 | 5 | ||
rs1465567 | 0.882 | 0.040 | 5 | 38370435 | missense variant | T/C | snv | 0.20 | 0.25 | 3 |