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 | 4 | 18016107 | intron variant | T/C | snv | 0.25 | 0.700 | 1.000 | 3 | 2008 | 2019 | ||||||
|
1 | 4 | 17875864 | synonymous variant | A/G | snv | 0.13 | 0.700 | 1.000 | 2 | 2015 | 2019 | ||||||
|
2 | 4 | 17943217 | intron variant | G/A | snv | 0.25 | 0.700 | 1.000 | 2 | 2008 | 2019 | ||||||
|
2 | 4 | 17944809 | intron variant | T/C | snv | 0.71 | 0.700 | 1.000 | 2 | 2010 | 2019 | ||||||
|
3 | 4 | 17991787 | intron variant | A/C | snv | 0.71 | 0.700 | 1.000 | 2 | 2011 | 2019 | ||||||
|
2 | 4 | 17935011 | intron variant | T/C | snv | 0.23 | 0.700 | 1.000 | 2 | 2014 | 2019 | ||||||
|
3 | 4 | 17918188 | intron variant | G/A | snv | 0.70 | 0.700 | 1.000 | 2 | 2012 | 2019 | ||||||
|
1 | 4 | 17996803 | intron variant | C/A | snv | 0.21 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
3 | 4 | 17940937 | intron variant | C/T | snv | 0.73 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 4 | 17963642 | intron variant | TT/-;T;TTT | delins | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1 | 4 | 17992675 | intron variant | T/C | snv | 0.12 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 4 | 17865243 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
2 | 4 | 17995443 | intron variant | G/A | snv | 0.25 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 4 | 17950585 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1 | 4 | 17878768 | intron variant | T/A | snv | 2.3E-04 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 4 | 17878793 | intron variant | A/C;G | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 4 | 17878849 | intron variant | T/A | snv | 1.7E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 |