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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
7 | 0.925 | 0.040 | 4 | 88962828 | intron variant | C/T | snv | 0.53 | 0.840 | 1.000 | 6 | 2010 | 2015 | ||||
|
11 | 0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 | 0.820 | 0.750 | 4 | 2010 | 2015 | ||||
|
3 | 1.000 | 0.040 | 4 | 88954758 | intron variant | C/T | snv | 0.45 | 0.800 | 1.000 | 1 | 2012 | 2012 | ||||
|
4 | 0.925 | 0.080 | 4 | 88965146 | intron variant | C/G;T | snv | 0.710 | 1.000 | 3 | 2010 | 2015 | |||||
|
9 | 1.000 | 0.040 | 4 | 88947927 | intron variant | C/T | snv | 0.47 | 0.700 | 1.000 | 2 | 2014 | 2019 | ||||
|
4 | 0.925 | 0.080 | 4 | 88945562 | intron variant | T/C | snv | 0.45 | 0.700 | 1.000 | 2 | 2014 | 2014 | ||||
|
4 | 0.925 | 0.040 | 4 | 88951941 | intron variant | A/G | snv | 0.47 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
2 | 1.000 | 0.040 | 4 | 88962667 | intron variant | G/A | snv | 0.59 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
3 | 1.000 | 0.040 | 4 | 88951025 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
1 | 1.000 | 0.040 | 4 | 88809748 | intron variant | T/C | snv | 6.7E-02 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
5 | 1.000 | 0.040 | 4 | 88963935 | intron variant | G/T | snv | 0.51 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
5 | 1.000 | 0.040 | 4 | 88855930 | 3 prime UTR variant | A/G | snv | 0.38 | 0.010 | 1.000 | 1 | 2013 | 2013 |