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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 0.827 | 0.120 | 19 | 44878777 | 3 prime UTR variant | A/G | snv | 0.58 | 0.800 | 1.000 | 2 | 2012 | 2019 | ||||
|
6 | 1.000 | 0.080 | 19 | 44885917 | intron variant | T/A | snv | 0.11 | 0.16 | 0.700 | 1.000 | 2 | 2012 | 2012 | |||
|
4 | 19 | 44886339 | intron variant | G/A | snv | 6.4E-02 | 0.700 | 1.000 | 2 | 2019 | 2019 | ||||||
|
3 | 19 | 44874210 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
3 | 19 | 44858317 | intron variant | G/A;C;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
4 | 1.000 | 0.080 | 19 | 44875803 | intron variant | A/C;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||
|
2 | 19 | 44870308 | intron variant | G/A | snv | 0.16 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
3 | 1.000 | 0.080 | 19 | 44879418 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
4 | 1.000 | 0.080 | 19 | 44854034 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||
|
2 | 19 | 44867911 | intron variant | G/A | snv | 0.44 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
6 | 1.000 | 0.080 | 19 | 44873027 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||
|
16 | 0.790 | 0.240 | 19 | 44888997 | 3 prime UTR variant | C/T | snv | 0.13 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
3 | 19 | 44869097 | intron variant | T/G | snv | 0.28 | 0.700 | 1.000 | 1 | 2012 | 2012 |