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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
12 | 0.807 | 0.240 | 5 | 75360714 | 3 prime UTR variant | T/C;G | snv | 0.37 | 0.800 | 1.000 | 10 | 2010 | 2019 | ||||
|
7 | 0.925 | 0.120 | 5 | 75352778 | intron variant | A/T | snv | 0.38 | 0.800 | 1.000 | 5 | 2008 | 2019 | ||||
|
12 | 0.763 | 0.280 | 5 | 75355259 | non coding transcript exon variant | A/G | snv | 0.50 | 0.58 | 0.800 | 1.000 | 4 | 2009 | 2019 | |||
|
3 | 5 | 75341886 | intron variant | A/T | snv | 0.38 | 0.800 | 1.000 | 3 | 2012 | 2019 | ||||||
|
2 | 5 | 75343434 | intron variant | T/G | snv | 0.35 | 0.700 | 1.000 | 3 | 2015 | 2019 | ||||||
|
7 | 0.882 | 0.120 | 5 | 75359901 | intron variant | C/T | snv | 0.35 | 0.800 | 1.000 | 3 | 2009 | 2019 | ||||
|
2 | 5 | 75340659 | intron variant | C/A | snv | 0.35 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
3 | 5 | 75348856 | intron variant | G/T | snv | 0.20 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
4 | 1.000 | 0.080 | 5 | 75352671 | intron variant | G/T | snv | 0.22 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
3 | 5 | 75335676 | intron variant | C/T | snv | 0.15 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 5 | 75343353 | intron variant | A/G | snv | 0.56 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
3 | 5 | 75348881 | intron variant | T/G | snv | 0.39 | 0.700 | 1.000 | 1 | 2012 | 2012 |