Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs78490412 | 1.000 | 0.040 | 2 | 143405256 | intron variant | C/T | snv | 0.22 | 1 | ||
rs13010737 | 1.000 | 0.040 | 2 | 143442474 | intron variant | G/A | snv | 0.36 | 1 | ||
rs6734367 | 2 | 143556678 | intron variant | T/A;G | snv | 1 | |||||
rs74847330 | 2 | 143074030 | intergenic variant | A/G | snv | 8.8E-02 | 4 | ||||
rs73962318 | 2 | 143097365 | non coding transcript exon variant | T/C | snv | 4.2E-02 | 2 |