Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7936323 | 0.882 | 0.160 | 11 | 76582714 | intergenic variant | G/A | snv | 0.44 | 6 | ||
rs61840192 | 1.000 | 0.080 | 10 | 9001441 | intergenic variant | G/A;C;T | snv | 3 | |||
rs10795656 | 1.000 | 0.080 | 10 | 8553876 | intergenic variant | G/A;T | snv | 4 | |||
rs4594881 | 1.000 | 0.080 | 5 | 35846713 | intergenic variant | G/T | snv | 0.28 | 2 | ||
rs7936312 | 0.882 | 0.080 | 11 | 76582682 | intergenic variant | G/T | snv | 0.44 | 5 | ||
rs112401631 | 0.882 | 0.120 | 17 | 40608272 | TF binding site variant | T/A | snv | 1.1E-02 | 8 | ||
rs1059513 | 0.776 | 0.240 | 12 | 57095926 | 3 prime UTR variant | T/C | snv | 8.0E-02 | 11 | ||
rs1837253 | 0.790 | 0.240 | 5 | 111066174 | upstream gene variant | T/C | snv | 0.72 | 10 | ||
rs2814778 | 0.763 | 0.360 | 1 | 159204893 | 5 prime UTR variant | T/C | snv | 0.25 | 24 | ||
rs9807989 | 1.000 | 0.080 | 2 | 102354740 | intron variant | T/C;G | snv | 0.46 | 2 | ||
rs3024971 | 0.827 | 0.200 | 12 | 57099944 | intron variant | T/G | snv | 7.8E-02 | 7.9E-02 | 7 |