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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
25 | 0.708 | 0.160 | 18 | 48927093 | intron variant | T/A;C | snv | 0.900 | 0.964 | 28 | 2007 | 2019 | |||||
|
18 | 0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 | 0.900 | 1.000 | 14 | 2007 | 2018 | ||||
|
13 | 0.763 | 0.080 | 18 | 48924606 | intron variant | A/G | snv | 0.87 | 0.820 | 1.000 | 6 | 2014 | 2019 | ||||
|
7 | 0.827 | 0.120 | 18 | 48932662 | intron variant | T/C | snv | 0.25 | 0.780 | 1.000 | 9 | 2007 | 2018 | ||||
|
11 | 0.763 | 0.080 | 18 | 48926786 | intron variant | A/T | snv | 0.50 | 0.730 | 1.000 | 5 | 2013 | 2019 | ||||
|
9 | 0.790 | 0.080 | 18 | 48927678 | intron variant | A/G;T | snv | 0.710 | 1.000 | 3 | 2012 | 2019 | |||||
|
9 | 0.790 | 0.080 | 18 | 48925503 | intron variant | G/A | snv | 0.47 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
9 | 0.790 | 0.080 | 18 | 48922435 | intron variant | T/C | snv | 0.54 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 1.000 | 0.080 | 18 | 48923195 | intron variant | C/A;G;T | snv | 0.020 | 1.000 | 2 | 2014 | 2016 | |||||
|
1 | 1.000 | 0.080 | 18 | 48920219 | 3 prime UTR variant | T/C | snv | 4.7E-02 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
3 | 0.882 | 0.120 | 18 | 48932953 | intron variant | C/T | snv | 0.52 | 0.010 | < 0.001 | 1 | 2014 | 2014 | ||||
|
3 | 1.000 | 0.080 | 18 | 48942576 | non coding transcript exon variant | G/A | snv | 0.14 | 0.13 | 0.010 | 1.000 | 1 | 2017 | 2017 |