Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 12 | ||
rs115829748 | 0.925 | 0.160 | 5 | 72098560 | intron variant | C/T | snv | 2.6E-02 | 2 | ||
rs143723948 | 0.925 | 0.160 | 9 | 37034098 | 5 prime UTR variant | C/T | snv | 2 | |||
rs28641753 | 0.925 | 0.160 | 3 | 104256574 | intergenic variant | C/T | snv | 4.5E-02 | 2 | ||
rs73018809 | 0.925 | 0.160 | 3 | 13329174 | intron variant | A/T | snv | 2.0E-02 | 2 |