Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9272346 | 0.790 | 0.320 | 6 | 32636595 | intron variant | G/A | snv | 0.54 | 6 | ||
rs2076530 | 0.724 | 0.640 | 6 | 32396039 | missense variant | T/C | snv | 0.42 | 0.40 | 5 | |
rs3806156 | 0.827 | 0.280 | 6 | 32405921 | intron variant | G/A;T | snv | 5 | |||
rs7775228 | 0.790 | 0.360 | 6 | 32690302 | TF binding site variant | T/C | snv | 0.15 | 5 | ||
rs9268645 | 0.827 | 0.360 | 6 | 32440750 | intron variant | C/G;T | snv | 5 | |||
rs9461799 | 0.807 | 0.360 | 6 | 32721752 | downstream gene variant | T/C | snv | 0.37 | 4 | ||
rs2239800 | 0.882 | 0.280 | 6 | 32745490 | intron variant | A/G | snv | 0.11 | 3 | ||
rs3101942 | 0.882 | 0.200 | 6 | 32902280 | intergenic variant | G/A;C | snv | 3 | |||
rs6903130 | 0.882 | 0.200 | 6 | 32764433 | upstream gene variant | G/A | snv | 0.53 | 3 | ||
rs415929 | 0.925 | 0.200 | 6 | 32221255 | synonymous variant | T/C | snv | 0.31 | 0.29 | 2 |