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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3 | 1 | 62652525 | intron variant | A/C;T | snv | 0.800 | 1.000 | 3 | 2009 | 2019 | |||||||
|
5 | 1 | 62560271 | intron variant | G/T | snv | 0.57 | 0.800 | 1.000 | 2 | 2010 | 2019 | ||||||
|
2 | 1 | 62583880 | intron variant | A/C;G | snv | 0.800 | 1.000 | 1 | 2013 | 2019 | |||||||
|
5 | 1 | 62465961 | intron variant | C/A | snv | 0.57 | 0.800 | 1.000 | 1 | 2012 | 2019 | ||||||
|
3 | 0.851 | 0.120 | 1 | 62583922 | intron variant | C/G;T | snv | 0.800 | 1.000 | 1 | 2012 | 2019 | |||||
|
5 | 1 | 62606594 | intron variant | A/C;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
2 | 1 | 62519226 | intron variant | C/T | snv | 0.34 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
5 | 1 | 62596235 | intron variant | C/T | snv | 0.39 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 1 | 62517220 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
2 | 1 | 62518022 | intron variant | A/C;G | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
2 | 1 | 62518080 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
2 | 1 | 62521284 | intron variant | C/A;T | snv | 0.58 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 1 | 62654700 | intron variant | C/T | snv | 0.57 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 1 | 62589609 | intron variant | G/A | snv | 0.12 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 1 | 62515769 | intron variant | G/A | snv | 0.57 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
5 | 1 | 62590441 | intron variant | G/A | snv | 0.42 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 1 | 62454337 | non coding transcript exon variant | A/G | snv | 0.36 | 0.700 | 1.000 | 1 | 2013 | 2013 |