Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 22 | |||
rs579459 | 0.752 | 0.320 | 9 | 133278724 | upstream gene variant | C/T | snv | 0.81 | 21 | ||
rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 14 | ||
rs529565 | 0.851 | 0.120 | 9 | 133274084 | intron variant | C/T | snv | 12 | |||
rs1799963 | 0.695 | 0.400 | 11 | 46739505 | 3 prime UTR variant | G/A | snv | 9.6E-03 | 10 | ||
rs4444878 | 0.851 | 0.120 | 4 | 186292729 | intron variant | C/A;T | snv | 7 | |||
rs7654093 | 0.882 | 0.120 | 4 | 154623920 | upstream gene variant | A/T | snv | 0.27 | 6 | ||
rs113092656 | 0.882 | 0.120 | 6 | 11615072 | intergenic variant | G/A | snv | 2.6E-02 | 5 | ||
rs114209171 | 0.882 | 0.120 | X | 155050522 | non coding transcript exon variant | T/C | snv | 0.23 | 5 | ||
rs17490626 | 0.882 | 0.120 | 10 | 69458890 | intron variant | G/C | snv | 8.4E-02 | 5 | ||
rs34234989 | 0.882 | 0.120 | 20 | 35186731 | intron variant | A/- | delins | 0.40 | 5 | ||
rs60942712 | 0.882 | 0.120 | 3 | 88998609 | intergenic variant | G/T | snv | 7.9E-02 | 5 | ||
rs72798544 | 0.882 | 0.120 | 2 | 42372465 | intron variant | T/G | snv | 1.3E-02 | 5 | ||
rs9797861 | 0.790 | 0.200 | 19 | 10632450 | intron variant | C/A;G;T | snv | 5 | |||
rs6825454 | 1.000 | 0.080 | 4 | 154580036 | downstream gene variant | T/C | snv | 0.25 | 3 |