Source: CURATED
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs569550 | 0.925 | 0.080 | 11 | 1865838 | intron variant | T/G | snv | 0.35 | 4 | ||
rs1973765 | 1.000 | 0.080 | 11 | 1877434 | intron variant | T/C | snv | 0.37 | 3 | ||
rs3817198 | 0.790 | 0.280 | 11 | 1887776 | intron variant | T/C | snv | 0.26 | 3 | ||
rs592373 | 0.925 | 0.080 | 11 | 1869760 | intron variant | G/A;T | snv | 0.63; 6.8E-06 | 3 | ||
rs4980383 | 1.000 | 0.080 | 11 | 1880867 | non coding transcript exon variant | C/T | snv | 0.37 | 1 |