Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10198175 | 0.925 | 0.080 | 2 | 20934123 | intergenic variant | A/G | snv | 0.93 | 3 | ||
rs111940429 | 0.925 | 0.080 | 2 | 107366232 | intron variant | C/A;T | snv | 2 | |||
rs145763646 | 0.925 | 0.080 | 3 | 66173478 | intron variant | G/A | snv | 0.13 | 2 | ||
rs17810023 | 0.925 | 0.080 | 6 | 80443056 | non coding transcript exon variant | C/T | snv | 1.7E-02 | 2 | ||
rs182107583 | 0.925 | 0.080 | 2 | 149675023 | intron variant | A/C | snv | 4.2E-03 | 2 | ||
rs1950038 | 0.925 | 0.080 | 2 | 183579642 | regulatory region variant | T/C | snv | 0.71 | 2 | ||
rs6006893 | 0.925 | 0.080 | 22 | 44858015 | intron variant | C/T | snv | 0.15 | 2 | ||
rs726170 | 0.925 | 0.080 | 22 | 44855931 | intron variant | C/T | snv | 0.15 | 2 | ||
rs73057489 | 0.925 | 0.080 | 12 | 17370820 | regulatory region variant | A/C | snv | 3.9E-02 | 2 | ||
rs7337127 | 0.925 | 0.080 | 13 | 104623579 | intergenic variant | C/A;T | snv | 2 | |||
rs76087671 | 0.925 | 0.080 | 20 | 24330541 | intergenic variant | C/A;G;T | snv | 2 | |||
rs7904579 | 0.925 | 0.080 | 10 | 17089754 | intron variant | G/A;C | snv | 2 |