Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs9303277 | 0.790 | 0.240 | 17 | 39820216 | intron variant | C/T | snv | 0.52 | 9 | ||
rs422112 | 1.000 | 0.080 | 17 | 45650771 | non coding transcript exon variant | G/A | snv | 0.14 | 3 | ||
rs5757611 | 1.000 | 0.080 | 22 | 39312352 | downstream gene variant | C/T | snv | 0.19 | 2 |