Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1059513 | 0.776 | 0.240 | 12 | 57095926 | 3 prime UTR variant | T/C | snv | 8.0E-02 | 11 | ||
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 | ||
rs12440045 | 0.925 | 0.080 | 15 | 41490486 | upstream gene variant | A/C | snv | 0.67 | 6 | ||
rs4821544 | 0.925 | 0.040 | 22 | 36862461 | intron variant | T/A;C | snv | 6 | |||
rs7936323 | 0.882 | 0.160 | 11 | 76582714 | intergenic variant | G/A | snv | 0.44 | 6 | ||
rs55646091 | 0.925 | 0.080 | 11 | 76588387 | upstream gene variant | G/A | snv | 3.0E-02 | 5 | ||
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 | 4 | ||
rs2381416 | 1.000 | 0.080 | 9 | 6193455 | upstream gene variant | C/A | snv | 0.65 | 4 | ||
rs1057258 | 2 | 233206983 | 3 prime UTR variant | C/T | snv | 0.30 | 3 | ||||
rs346835 | 2 | 8298563 | intron variant | C/T | snv | 0.39 | 3 | ||||
rs6021268 | 20 | 51524602 | intron variant | T/C | snv | 5.8E-02 | 3 |