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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
15 | 0.763 | 0.200 | 15 | 28120472 | intron variant | A/G | snv | 0.50 | 0.800 | 1.000 | 4 | 2010 | 2013 | ||||
|
5 | 15 | 28285036 | intron variant | C/A;T | snv | 0.800 | 1.000 | 4 | 2007 | 2018 | |||||||
|
5 | 1.000 | 0.080 | 15 | 28268218 | intron variant | T/C;G | snv | 0.800 | 1.000 | 2 | 2008 | 2013 | |||||
|
8 | 0.851 | 0.120 | 15 | 28111713 | 3 prime UTR variant | C/T | snv | 0.49 | 0.50 | 0.700 | 1.000 | 1 | 2013 | 2013 | |||
|
2 | 15 | 28141480 | synonymous variant | C/T | snv | 0.25 | 0.26 | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 15 | 28114112 | intron variant | G/A | snv | 0.78 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
3 | 1.000 | 0.040 | 15 | 28290120 | intron variant | A/C | snv | 0.77 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
2 | 15 | 28281082 | intron variant | G/A | snv | 0.23 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 15 | 28128866 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
3 | 15 | 28243742 | intron variant | T/C | snv | 0.16 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
3 | 15 | 28270938 | intron variant | C/T | snv | 0.65 | 0.700 | 1.000 | 1 | 2012 | 2012 |