Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs386794162 | 0.925 | 0.160 | 16 | 89935711 | missense variant | CG/GA | mnv | 2 | |||
rs758216329 | 1.000 | 0.080 | 1 | 155958388 | missense variant | C/T | snv | 1.2E-05 | 1 | ||
rs1421508093 | 1.000 | 0.080 | 15 | 79025460 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1064793286 | 1.000 | 0.080 | 12 | 49185198 | missense variant | G/A;C | snv | 1 |