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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 0.776 | 0.280 | 10 | 121577821 | intron variant | A/G | snv | 0.53 | 0.740 | 1.000 | 5 | 2009 | 2017 | ||||
|
1 | 0.695 | 0.360 | 10 | 121592803 | intron variant | A/G | snv | 0.58 | 0.800 | 0.972 | 2 | 2007 | 2019 | ||||
|
1 | 0.716 | 0.320 | 10 | 121586676 | intron variant | A/G;T | snv | 0.800 | 1.000 | 4 | 2007 | 2018 | |||||
|
1 | 1.000 | 0.080 | 10 | 121589810 | intron variant | A/T | snv | 3.6E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 0.851 | 0.080 | 10 | 121580918 | intron variant | C/- | delins | 0.710 | 1.000 | 1 | 2016 | 2017 | |||||
|
1 | 0.925 | 0.080 | 10 | 121580797 | intron variant | C/A;T | snv | 0.790 | 0.909 | 2 | 2009 | 2018 | |||||
|
2 | 1.000 | 0.080 | 10 | 121592706 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
1 | 0.851 | 0.080 | 10 | 121573063 | intron variant | C/G;T | snv | 0.720 | 1.000 | 1 | 2009 | 2012 | |||||
|
1 | 1.000 | 0.080 | 10 | 121568362 | intron variant | C/T | snv | 0.19 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
2 | 0.882 | 0.160 | 10 | 121594355 | intron variant | C/T | snv | 0.54 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
3 | 0.882 | 0.120 | 10 | 121586602 | intron variant | G/A | snv | 0.54 | 0.710 | 1.000 | 1 | 2010 | 2010 | ||||
|
17 | 0.695 | 0.280 | 10 | 121575416 | intron variant | G/A;T | snv | 0.34 | 0.720 | 1.000 | 1 | 2012 | 2016 | ||||
|
1 | 0.925 | 0.080 | 10 | 121589148 | intron variant | T/A;G | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
1 | 0.851 | 0.160 | 10 | 121591810 | intron variant | T/C | snv | 0.56 | 0.770 | 1.000 | 1 | 2009 | 2017 |