Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10667251 | 0.925 | 0.080 | 17 | 49388381 | intron variant | -/TCT | delins | 0.47 | 4 | ||
rs10795656 | 1.000 | 0.080 | 10 | 8553876 | intergenic variant | G/A;T | snv | 4 | |||
rs2033784 | 1.000 | 0.080 | 15 | 67157322 | intron variant | A/G | snv | 0.35 | 3 | ||
rs2381416 | 1.000 | 0.080 | 9 | 6193455 | upstream gene variant | C/A | snv | 0.65 | 3 | ||
rs3785356 | 0.925 | 0.080 | 16 | 27337847 | intron variant | C/T | snv | 0.25 | 5 | ||
rs55646091 | 0.925 | 0.080 | 11 | 76588387 | upstream gene variant | G/A | snv | 3.0E-02 | 5 | ||
rs61840192 | 1.000 | 0.080 | 10 | 9001441 | intergenic variant | G/A;C;T | snv | 3 | |||
rs112401631 | 0.882 | 0.120 | 17 | 40608272 | TF binding site variant | T/A | snv | 1.1E-02 | 8 | ||
rs34290285 | 0.851 | 0.120 | 2 | 241759225 | intron variant | G/A | snv | 0.27 | 8 | ||
rs7936323 | 0.882 | 0.160 | 11 | 76582714 | intergenic variant | G/A | snv | 0.44 | 6 | ||
rs11065979 | 0.851 | 0.200 | 12 | 111621753 | intergenic variant | C/T | snv | 0.30 | 12 | ||
rs1059513 | 0.776 | 0.240 | 12 | 57095926 | 3 prime UTR variant | T/C | snv | 8.0E-02 | 6 |