Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2082940 | 0.763 | 0.480 | 3 | 186856375 | 3 prime UTR variant | T/A;C | snv | 10 | |||
rs5030772 | 0.790 | 0.320 | 1 | 172664210 | intron variant | A/G | snv | 9.9E-02 | 7 | ||
rs7775228 | 0.790 | 0.360 | 6 | 32690302 | TF binding site variant | T/C | snv | 0.15 | 7 | ||
rs2929970 | 0.827 | 0.200 | 8 | 133228894 | 3 prime UTR variant | G/A | snv | 0.52 | 5 | ||
rs7135617 | 0.827 | 0.240 | 12 | 121631099 | intron variant | T/C;G | snv | 5 | |||
rs2289263 | 0.925 | 0.120 | 15 | 67146869 | intron variant | T/G | snv | 0.43 | 3 | ||
rs3219463 | 0.925 | 0.120 | 1 | 45340760 | 5 prime UTR variant | C/T | snv | 0.27 | 2 | ||
rs6494629 | 0.925 | 0.120 | 15 | 67081773 | intron variant | C/T | snv | 0.52 | 2 |