Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2287161 | 0.827 | 0.080 | 12 | 106987362 | upstream gene variant | C/G;T | snv | 7 | |||
rs10838524 | 0.851 | 0.120 | 11 | 45848626 | intron variant | A/G | snv | 0.42 | 5 | ||
rs11541353 | 0.851 | 0.120 | 2 | 100977729 | missense variant | C/T | snv | 0.14 | 0.14 | 4 | |
rs2314339 | 0.851 | 0.120 | 17 | 40096959 | intron variant | C/T | snv | 0.20 | 4 | ||
rs2028122 | 0.851 | 0.120 | 15 | 60549076 | intron variant | A/G | snv | 0.51 | 4 |