Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11205303 | 0.882 | 0.120 | 1 | 149934520 | missense variant | T/C | snv | 0.33 | 0.29 | 8 | |
rs3791679 | 0.925 | 0.120 | 2 | 55869757 | intron variant | A/G | snv | 0.20 | 8 | ||
rs55872725 | 16 | 53775211 | intron variant | C/T | snv | 0.31 | 6 | ||||
rs3817428 | 15 | 88872016 | missense variant | C/G | snv | 0.20 | 0.20 | 3 | |||
rs481806 | 7 | 28167681 | intron variant | G/T | snv | 0.77 | 2 |