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 | 0.790 | 0.320 | 11 | 2818521 | intron variant | C/T | snv | 9.2E-02 | 0.900 | 1.000 | 6 | 2008 | 2019 | ||||
|
1 | 0.790 | 0.240 | 11 | 2835964 | intron variant | A/C;T | snv | 0.900 | 0.889 | 2 | 2008 | 2019 | |||||
|
2 | 0.882 | 0.200 | 11 | 2837316 | intron variant | C/T | snv | 8.1E-02 | 0.880 | 1.000 | 3 | 2008 | 2019 | ||||
|
1 | 1.000 | 0.080 | 11 | 2670241 | non coding transcript exon variant | A/G | snv | 0.62 | 0.840 | 1.000 | 3 | 2010 | 2019 | ||||
|
1 | 1.000 | 0.080 | 11 | 2825839 | intron variant | T/G | snv | 0.40 | 0.810 | 1.000 | 4 | 2010 | 2018 | ||||
|
1 | 1.000 | 0.080 | 11 | 2837210 | intron variant | G/A;T | snv | 0.810 | 1.000 | 3 | 2011 | 2019 | |||||
|
1 | 1.000 | 0.080 | 11 | 2817183 | intron variant | T/C | snv | 0.45 | 0.810 | 1.000 | 1 | 2010 | 2017 | ||||
|
1 | 0.882 | 0.160 | 11 | 2822986 | intron variant | G/A;C | snv | 0.810 | 1.000 | 1 | 2011 | 2016 | |||||
|
1 | 1.000 | 0.080 | 11 | 2670270 | non coding transcript exon variant | G/A | snv | 0.31 | 0.800 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 1.000 | 0.080 | 11 | 2810311 | intron variant | T/C | snv | 0.12 | 0.800 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 1.000 | 0.080 | 11 | 2828300 | intron variant | A/C | snv | 0.10 | 0.760 | 1.000 | 2 | 2009 | 2017 | ||||
|
1 | 1.000 | 0.080 | 11 | 2620807 | non coding transcript exon variant | A/G | snv | 5.5E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 0.925 | 0.080 | 11 | 2684113 | non coding transcript exon variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
1 | 1.000 | 0.080 | 11 | 2822573 | intron variant | G/A | snv | 0.22 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.080 | 11 | 2836784 | intron variant | C/G | snv | 2.3E-04 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.080 | 11 | 2619190 | non coding transcript exon variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 |