Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6065904 | 1.000 | 0.080 | 20 | 45906012 | intron variant | G/A | snv | 0.23 | 4 | ||
rs6065906 | 20 | 45925376 | downstream gene variant | T/A;C;G | snv | 4 | |||||
rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 10 | ||
rs4803750 | 0.807 | 0.240 | 19 | 44744370 | upstream gene variant | A/G | snv | 7.7E-02 | 6 | ||
rs1160985 | 1.000 | 0.080 | 19 | 44900155 | intron variant | C/T | snv | 0.52 | 5 | ||
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 5 | |
rs17249141 | 19 | 11089332 | upstream gene variant | C/T | snv | 3.3E-03 | 2 | ||||
rs55791371 | 0.925 | 0.080 | 19 | 11077477 | intron variant | A/C | snv | 0.11 | 1 | ||
rs4939883 | 1.000 | 0.040 | 18 | 49640844 | TF binding site variant | T/C;G | snv | 3 | |||
rs7228085 | 18 | 49634444 | intergenic variant | A/G | snv | 0.53 | 1 | ||||
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 11 | ||
rs1864163 | 0.882 | 0.120 | 16 | 56963321 | intron variant | G/A | snv | 0.26 | 8 | ||
rs1532624 | 0.851 | 0.160 | 16 | 56971567 | intron variant | C/A | snv | 0.34 | 7 | ||
rs1800775 | 0.790 | 0.240 | 16 | 56961324 | upstream gene variant | C/A;G | snv | 0.51; 5.7E-06 | 7 | ||
rs7499892 | 16 | 56972678 | intron variant | C/G;T | snv | 6 | |||||
rs11075253 | 16 | 15054789 | intron variant | C/A | snv | 0.22 | 1 | ||||
rs11644601 | 16 | 15078261 | intron variant | T/C | snv | 0.21 | 1 | ||||
rs1532085 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 9 | |||
rs35853021 | 15 | 58388444 | intron variant | G/T | snv | 0.38 | 1 | ||||
rs17267292 | 13 | 92670893 | intron variant | T/C | snv | 0.22 | 1 | ||||
rs174547 | 0.742 | 0.240 | 11 | 61803311 | intron variant | T/C | snv | 0.28 | 10 | ||
rs651821 | 0.851 | 0.360 | 11 | 116791863 | 5 prime UTR variant | C/T | snv | 0.88 | 0.89 | 6 | |
rs2229738 | 11 | 68794860 | missense variant | C/G;T | snv | 6.3E-02 | 2 | ||||
rs2575876 | 9 | 104903458 | intron variant | G/A | snv | 0.24 | 4 | ||||
rs6982636 | 8 | 125467073 | intron variant | G/A | snv | 0.43 | 6 |