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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5 | 1.000 | 2 | 49264671 | intron variant | G/A | snv | 0.26 | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
1 | 4 | 65271097 | intergenic variant | C/T | snv | 0.33 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
5 | 0.851 | 0.080 | 1 | 4034008 | regulatory region variant | C/T | snv | 8.6E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
3 | 0.925 | 0.120 | 2 | 166773339 | regulatory region variant | C/T | snv | 0.13 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
3 | 1.000 | 0.120 | 2 | 67075611 | intergenic variant | A/G | snv | 0.25 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 1 | 22551320 | intergenic variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
3 | 1.000 | 0.120 | 9 | 32867483 | intron variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 1.000 | 20 | 945754 | intergenic variant | G/A | snv | 0.29 | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
5 | 1.000 | X | 144281548 | intergenic variant | C/A;G;T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||
|
7 | 0.807 | 0.240 | 4 | 53790270 | intron variant | G/A | snv | 2.5E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
5 | 1.000 | 18 | 8931654 | intergenic variant | T/C | snv | 0.19 | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
5 | 1.000 | 1 | 182052148 | downstream gene variant | C/T | snv | 8.5E-02 | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
1 | 12 | 73435176 | intergenic variant | C/T | snv | 0.59 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
|
5 | 1.000 | 2 | 194682669 | intergenic variant | G/A | snv | 0.94 | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
5 | 1.000 | 2 | 194695273 | intergenic variant | A/C;T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||
|
5 | 1.000 | 6 | 221146 | intergenic variant | G/A | snv | 2.6E-02 | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
5 | 1.000 | 2 | 49270867 | intron variant | G/A | snv | 0.25 | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
214 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
|
4 | 0.882 | 0.040 | 2 | 73909130 | missense variant | C/A;T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
52 | 0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv | 0.010 | < 0.001 | 1 | 2013 | 2013 | |||||
|
6 | 0.851 | 0.240 | 14 | 50628394 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 0.010 | 1.000 | 1 | 2007 | 2007 | |||
|
11 | 0.776 | 0.160 | 10 | 119672373 | missense variant | C/A;T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
3 | 1.000 | 0.080 | 10 | 130032376 | intron variant | A/C;T | snv | 0.21 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
7 | 0.807 | 0.160 | 22 | 23767438 | missense variant | C/A;T | snv | 1.8E-05; 4.4E-06 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 15 | 101178712 | missense variant | A/G | snv | 1.2E-05 | 0.010 | 1.000 | 1 | 2013 | 2013 |