Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6009 | 1.000 | 0.080 | 1 | 169529596 | intron variant | T/A;C | snv | 0.94 | 3 | ||
rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 3 | ||
rs6427196 | 1.000 | 0.080 | 1 | 169511985 | 3 prime UTR variant | C/G;T | snv | 3 | |||
rs2038024 | 1.000 | 0.080 | 1 | 169486744 | non coding transcript exon variant | C/A | snv | 0.88 | 2 |