Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.040 | 9 | 114907019 | intron variant | A/G | snv | 0.58 | 0.700 | 1.000 | 1 | 2005 | 2005 | ||||
|
1 | 1.000 | 0.040 | 9 | 114856029 | intron variant | A/C | snv | 7.2E-02 | 0.700 | 1.000 | 1 | 2005 | 2005 | ||||
|
1 | 1.000 | 0.040 | 9 | 114917522 | intron variant | G/A | snv | 0.21 | 0.700 | 1.000 | 1 | 2005 | 2005 | ||||
|
1 | 1.000 | 0.040 | 9 | 114901931 | intron variant | T/C | snv | 0.56 | 0.700 | 1.000 | 1 | 2005 | 2005 | ||||
|
1 | 1.000 | 0.040 | 9 | 114901892 | intron variant | T/C | snv | 0.56 | 0.700 | 1.000 | 1 | 2005 | 2005 | ||||
|
1 | 1.000 | 0.040 | 9 | 114929278 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 1.000 | 0.040 | 9 | 114905163 | intron variant | T/C | snv | 0.21 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.040 | 9 | 114915956 | intron variant | T/C | snv | 0.58 | 0.700 | 1.000 | 1 | 2005 | 2005 | ||||
|
1 | 1.000 | 0.040 | 9 | 114907419 | intron variant | A/T | snv | 0.22 | 0.700 | 1.000 | 1 | 2005 | 2005 | ||||
|
1 | 0.925 | 0.080 | 9 | 114867763 | intron variant | C/T | snv | 0.52 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 0.925 | 0.080 | 9 | 114880138 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2013 | 2013 |