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 | 1.000 | 0.080 | 2 | 70790637 | start lost | A/G | snv | 3.5E-05 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.080 | 17 | 43094660 | missense variant | A/C | snv | 7.0E-06 | 0.010 | < 0.001 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.080 | 2 | 48968759 | missense variant | T/C | snv | 4.0E-06 | 2.8E-05 | 0.010 | 1.000 | 1 | 2019 | 2019 | |||
|
1 | 1.000 | 0.080 | 2 | 49068268 | stop gained | G/A | snv | 7.0E-06 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.080 | 2 | 48962622 | 3 prime UTR variant | A/G | snv | 7.4E-04 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.080 | 1 | 34795159 | missense variant | G/A | snv | 2.1E-03 | 8.4E-03 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||
|
1 | 1.000 | 0.080 | 19 | 2251138 | missense variant | C/G;T | snv | 1.1E-03; 7.5E-06 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
2 | 1.000 | 0.080 | 6 | 43524840 | synonymous variant | G/A | snv | 0.30 | 0.26 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||
|
1 | 1.000 | 0.080 | 4 | 155136200 | intergenic variant | G/A | snv | 0.70 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 1.000 | 0.080 | 4 | 83463563 | missense variant | G/C | snv | 2.4E-05 | 3.5E-05 | 0.010 | < 0.001 | 1 | 2019 | 2019 | |||
|
1 | 1.000 | 0.080 | 20 | 5984849 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 | 0.010 | 1.000 | 1 | 2016 | 2016 | |||
|
2 | 1.000 | 0.080 | 14 | 55440454 | missense variant | C/A;G;T | snv | 4.0E-06; 0.63; 4.0E-06 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 1.000 | 0.080 | 2 | 200571796 | frameshift variant | GA/- | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 2 | 219575194 | missense variant | G/A | snv | 2.3E-02 | 1.7E-02 | 0.080 | 0.625 | 8 | 2002 | 2014 | |||
|
2 | 0.925 | 0.080 | 6 | 32976646 | missense variant | G/A | snv | 4.1E-06 | 0.030 | 0.667 | 3 | 2006 | 2010 | ||||
|
2 | 0.925 | 0.080 | X | 50916280 | synonymous variant | C/T | snv | 5.8E-02 | 0.14 | 0.020 | 1.000 | 2 | 2015 | 2019 | |||
|
3 | 0.925 | 0.080 | 5 | 129721066 | intron variant | G/T | snv | 0.94 | 0.710 | 1.000 | 2 | 2009 | 2013 | ||||
|
2 | 0.925 | 0.080 | 5 | 132862507 | synonymous variant | G/A | snv | 0.52 | 0.50 | 0.020 | 1.000 | 2 | 2007 | 2015 | |||
|
2 | 0.925 | 0.080 | 8 | 100800928 | intergenic variant | A/G | snv | 0.13 | 0.810 | 1.000 | 2 | 2012 | 2014 | ||||
|
2 | 0.925 | 0.160 | X | 50916132 | missense variant | A/C;G | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
2 | 0.925 | 0.080 | 12 | 6777854 | missense variant | T/C | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
2 | 0.925 | 0.080 | 6 | 31759476 | missense variant | G/T | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
|
4 | 0.925 | 0.120 | 19 | 55322296 | intron variant | A/G | snv | 0.35 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
2 | 0.925 | 0.080 | 7 | 33349101 | missense variant | G/A | snv | 0.21 | 0.18 | 0.010 | 1.000 | 1 | 2008 | 2008 | |||
|
2 | 0.925 | 0.080 | 19 | 55288961 | intron variant | T/A;C | snv | 0.010 | 1.000 | 1 | 2014 | 2014 |