Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs34560261 | 0.882 | 0.040 | 15 | 90191194 | intron variant | C/T | snv | 0.12 | 3 | ||
rs112115472 | 0.925 | 7 | 13606234 | intron variant | C/T | snv | 2.0E-02 | 2 | |||
rs2523616 | 0.925 | 6 | 31352785 | intron variant | T/C | snv | 0.84 | 2 | |||
rs34097647 | 0.925 | 6 | 151108937 | intron variant | C/T | snv | 0.16 | 2 | |||
rs62388754 | 0.925 | 6 | 30033926 | intron variant | C/T | snv | 4.9E-02 | 2 | |||
rs6731286 | 0.925 | 2 | 62612684 | intron variant | A/G;T | snv | 2 | ||||
rs760327 | 0.925 | 8 | 133490986 | intron variant | G/C | snv | 0.59 | 2 | |||
rs8065764 | 0.925 | 17 | 21103149 | intergenic variant | T/A;C | snv | 2 | ||||
rs1800440 | 0.653 | 0.440 | 2 | 38070996 | missense variant | T/C;G | snv | 0.15; 4.0E-06 | 29 | ||
rs6471 | 0.683 | 0.360 | 6 | 32040110 | missense variant | G/A;C;T | snv | 1.2E-05; 5.3E-03 | 24 | ||
rs147324178 | 0.925 | 6 | 31356965 | splice region variant | T/A;C | snv | 9.2E-05; 0.85 | 2 | |||
rs10045403 | 0.882 | 0.040 | 5 | 96812030 | upstream gene variant | A/G | snv | 0.23 | 3 | ||
rs111463574 | 0.925 | 12 | 95005582 | upstream gene variant | C/T | snv | 8.1E-02 | 2 | |||
rs7749944 | 0.925 | 6 | 29992223 | upstream gene variant | A/C | snv | 1.3E-02 | 2 |