Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4467099 | 16 | 11449038 | missense variant | C/A;T | snv | 0.66 | 1 | ||||
rs352140 | 0.630 | 0.680 | 3 | 52222681 | synonymous variant | C/A;G;T | snv | 2.0E-05; 0.49 | 42 | ||
rs10853728 | 0.851 | 0.160 | 19 | 39254506 | downstream gene variant | C/A;G;T | snv | 5 | |||
rs1127354 | 0.667 | 0.400 | 20 | 3213196 | missense variant | C/A;G | snv | 7.5E-02 | 26 | ||
rs4803217 | 0.882 | 0.120 | 19 | 39243580 | 3 prime UTR variant | C/A | snv | 0.39 | 4 | ||
rs17568725 | 5 | 171743637 | TF binding site variant | C/A | snv | 0.19 | 1 | ||||
rs2174866 | 15 | 53172023 | intergenic variant | A/T | snv | 6.2E-02 | 1 | ||||
rs7518687 | 1 | 168663745 | intergenic variant | A/T | snv | 0.22 | 1 | ||||
rs8014067 | 14 | 62086539 | intron variant | A/T | snv | 0.79 | 1 | ||||
rs1432133 | 15 | 26983199 | intron variant | A/G;T | snv | 1 | |||||
rs3746444 | 0.514 | 0.760 | 20 | 34990448 | mature miRNA variant | A/G | snv | 0.20 | 0.19 | 105 | |
rs187084 | 0.641 | 0.480 | 3 | 52227015 | intron variant | A/G | snv | 0.38 | 36 | ||
rs12980275 | 0.701 | 0.360 | 19 | 39241143 | upstream gene variant | A/G | snv | 0.36 | 23 | ||
rs1898830 | 0.807 | 0.280 | 4 | 153687301 | intron variant | A/G | snv | 0.30 | 10 | ||
rs3087943 | 6 | 24650533 | 3 prime UTR variant | A/G | snv | 0.18 | 1 | ||||
rs7270101 | 0.776 | 0.200 | 20 | 3213247 | intron variant | A/C | snv | 8.7E-02 | 9.7E-02 | 10 | |
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 |