Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 30 | |
rs115560420 | 3 | 67375539 | 3 prime UTR variant | G/T | snv | 8.8E-02 | 2 | ||||
rs4894797 | 3 | 172065756 | intron variant | G/A | snv | 0.47 | 2 | ||||
rs2277339 | 12 | 56752285 | missense variant | T/G | snv | 0.12 | 0.14 | 10 | |||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 29 | |
rs2072153 | 17 | 49312652 | intron variant | G/A;C | snv | 3.7E-04; 0.33 | 3 | ||||
rs74929147 | 19 | 18302251 | downstream gene variant | G/A;C | snv | 4 | |||||
rs1279683 | 1.000 | 0.040 | 20 | 5002446 | intron variant | G/A;C | snv | 2 | |||
rs6121246 | 20 | 31845549 | 5 prime UTR variant | C/T | snv | 0.20 | 0.29 | 2 |