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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 0.827 | 0.240 | 6 | 20679478 | intron variant | A/G;T | snv | 0.900 | 0.966 | 6 | 2007 | 2019 | |||||
|
2 | 0.807 | 0.200 | 6 | 20661019 | intron variant | G/A;C;T | snv | 0.900 | 0.958 | 5 | 2007 | 2019 | |||||
|
1 | 0.827 | 0.160 | 6 | 20660803 | intron variant | A/C | snv | 0.40 | 0.900 | 1.000 | 2 | 2007 | 2019 | ||||
|
1 | 0.925 | 0.120 | 6 | 20657333 | intron variant | A/G | snv | 0.41 | 0.830 | 1.000 | 2 | 2009 | 2019 | ||||
|
1 | 0.882 | 0.120 | 6 | 20717024 | intron variant | T/C | snv | 0.30 | 0.830 | 1.000 | 2 | 2007 | 2017 | ||||
|
1 | 1.000 | 0.080 | 6 | 20687890 | intron variant | T/A;G | snv | 0.26 | 0.820 | 1.000 | 2 | 2010 | 2019 | ||||
|
1 | 0.925 | 0.120 | 6 | 20657634 | intron variant | A/G | snv | 0.40 | 0.820 | 1.000 | 1 | 2008 | 2019 | ||||
|
2 | 0.925 | 0.120 | 6 | 20703721 | intron variant | A/G | snv | 0.27 | 0.820 | 1.000 | 1 | 2007 | 2012 | ||||
|
1 | 1.000 | 0.080 | 6 | 20686342 | intron variant | C/A | snv | 0.25 | 0.800 | 1.000 | 3 | 2011 | 2016 | ||||
|
1 | 1.000 | 0.080 | 6 | 20641105 | intron variant | C/T | snv | 0.13 | 0.800 | 1.000 | 1 | 2010 | 2013 | ||||
|
1 | 1.000 | 0.080 | 6 | 20719330 | intron variant | G/A | snv | 0.30 | 0.800 | 1.000 | 1 | 2011 | 2019 | ||||
|
2 | 1.000 | 0.080 | 6 | 20682391 | intron variant | T/C | snv | 0.29 | 0.710 | 1.000 | 1 | 2016 | 2019 | ||||
|
3 | 1.000 | 0.080 | 6 | 20675561 | intron variant | C/A | snv | 0.26 | 0.700 | 1.000 | 1 | 2018 | 2018 |