Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs1042114 | 0.807 | 0.120 | 1 | 28812463 | missense variant | G/C;T | snv | 0.91 | 6 | ||
rs6454674 | 0.851 | 0.120 | 6 | 88163211 | intron variant | T/G | snv | 0.32 | 5 | ||
rs13273442 | 0.882 | 0.080 | 8 | 42688874 | intergenic variant | A/G | snv | 0.66 | 4 | ||
rs2629540 | 0.925 | 0.080 | 10 | 124737579 | intron variant | G/C | snv | 0.18 | 4 | ||
rs2952621 | 0.882 | 0.080 | 2 | 129240870 | downstream gene variant | T/A;C | snv | 4 | |||
rs1868152 | 0.925 | 0.080 | 3 | 186502274 | intergenic variant | A/G;T | snv | 0.85 | 2 |