Source: INFERRED ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 31 | |
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 26 | ||
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 22 | |
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 15 | |||||
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 14 | ||
rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
rs2853961 | 6 | 31264212 | downstream gene variant | G/A | snv | 0.38 | 13 | ||||
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 | ||
rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
rs3840870 | 17 | 50184820 | 3 prime UTR variant | -/CTTG | delins | 13 | |||||
rs4837892 | 9 | 121826025 | intron variant | G/T | snv | 0.36 | 13 | ||||
rs7296503 | 12 | 41306962 | intron variant | C/T | snv | 0.57 | 13 | ||||
rs76792961 | 16 | 243594 | intron variant | C/T | snv | 7.3E-03 | 13 | ||||
rs7776054 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 13 | ||||
rs9917425 | 20 | 16755400 | intron variant | G/T | snv | 0.16 | 13 | ||||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs140522 | 0.851 | 0.160 | 22 | 50532837 | upstream gene variant | T/A;C | snv | 11 | |||
rs2277339 | 12 | 56752285 | missense variant | T/G | snv | 0.12 | 0.14 | 10 | |||
rs35979828 | 12 | 54292096 | intron variant | C/T | snv | 5.0E-02 | 9 | ||||
rs17476364 | 10 | 69334748 | intron variant | T/C | snv | 6.4E-02 | 8 | ||||
rs2075672 | 7 | 100642673 | intron variant | A/G | snv | 0.65 | 8 | ||||
rs9487023 | 6 | 109268801 | intron variant | A/G | snv | 0.40 | 8 | ||||
rs1050828 | 0.790 | 0.200 | X | 154536002 | missense variant | C/T | snv | 9.1E-03 | 3.6E-02 | 7 |