Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13000344 | 0.925 | 0.040 | 2 | 63062599 | downstream gene variant | T/G | snv | 0.11 | 2 | ||
rs1409313 | 1.000 | 0.040 | 10 | 102431844 | intron variant | T/C | snv | 0.85 | 2 | ||
rs155806 | 1.000 | 0.040 | 5 | 140970255 | intron variant | A/G | snv | 8.9E-02 | 2 | ||
rs1559619762 | 1.000 | 0.040 | 3 | 70977827 | splice donor variant | C/G | snv | 2 | |||
rs1861972 | 0.925 | 0.040 | 7 | 155461298 | intron variant | G/A | snv | 0.72 | 2 | ||
rs1861973 | 0.925 | 0.040 | 7 | 155461450 | intron variant | T/C | snv | 0.73 | 2 | ||
rs1881084 | 0.925 | 0.040 | 7 | 127704626 | intron variant | G/A | snv | 0.33 | 2 | ||
rs1882260 | 1.000 | 0.040 | X | 5890820 | 3 prime UTR variant | G/A | snv | 2 | |||
rs1912960 | 0.925 | 0.040 | 4 | 46951864 | intron variant | G/C | snv | 0.28 | 2 | ||
rs2018650 | 0.925 | 0.040 | 2 | 63045589 | 3 prime UTR variant | T/C | snv | 0.11 | 2 | ||
rs2278556 | 0.925 | 0.040 | 3 | 10360419 | intron variant | G/A | snv | 0.34 | 2 | ||
rs2351299 | 1.000 | 0.040 | 4 | 47141348 | intron variant | G/T | snv | 0.19 | 2 | ||
rs237889 | 0.925 | 0.040 | 3 | 8760797 | intron variant | T/C | snv | 0.71 | 2 | ||
rs25925 | 0.925 | 0.040 | 5 | 111484055 | synonymous variant | G/C | snv | 0.75 | 0.83 | 2 | |
rs2896218 | 0.925 | 0.040 | 7 | 117279924 | intron variant | G/A | snv | 0.60 | 2 | ||
rs301434 | 0.925 | 0.040 | 9 | 4582082 | intron variant | C/G;T | snv | 2 | |||
rs301979 | 0.925 | 0.040 | 9 | 4576851 | intron variant | G/A;C | snv | 2 | |||
rs34808376 | 0.925 | 0.040 | 7 | 155456016 | intron variant | -/GC | delins | 2 | |||
rs35424709 | 0.925 | 0.040 | 3 | 193454190 | missense variant | T/A | snv | 8.6E-02 | 7.8E-02 | 2 | |
rs35678 | 0.925 | 0.040 | 3 | 10338239 | missense variant | C/T | snv | 0.49 | 0.47 | 2 | |
rs370911031 | 0.925 | 0.040 | 9 | 130219801 | missense variant | G/A | snv | 1.5E-04 | 8.4E-05 | 2 | |
rs3735653 | 0.925 | 0.040 | 7 | 155458738 | missense variant | C/G;T | snv | 0.54 | 2 | ||
rs3832300 | 1.000 | 0.040 | 4 | 47426318 | 3 prime UTR variant | -/T | delins | 5.1E-02 | 2 | ||
rs4482737 | 1.000 | 0.040 | 4 | 47320173 | missense variant | T/C;G | snv | 0.99; 4.0E-06 | 2 | ||
rs4773054 | 1.000 | 0.040 | 13 | 109501681 | intron variant | T/C | snv | 0.89 | 2 |