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 | 1.000 | 0.040 | X | 106928709 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.200 | 22 | 37973567 | inframe deletion | CTGGGGTCAGAGATG/- | delins | 0.700 | 0 | ||||||||
|
6 | 0.827 | 0.160 | 2 | 176094518 | stop gained | C/T | snv | 8.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
2 | 1.000 | 8 | 30846888 | stop gained | A/C | snv | 0.700 | 0 | |||||||||
|
3 | 0.925 | 0.040 | 9 | 25677217 | 3 prime UTR variant | T/C | snv | 0.44 | 0.010 | < 0.001 | 1 | 2018 | 2018 | ||||
|
4 | 0.925 | 0.120 | 5 | 132369766 | 5 prime UTR variant | C/G | snv | 0.59 | 0.010 | < 0.001 | 1 | 2015 | 2015 | ||||
|
1 | 9 | 24545697 | 5 prime UTR variant | G/C | snv | 0.25 | 0.25 | 0.010 | < 0.001 | 1 | 2018 | 2018 | |||||
|
1 | 19 | 43416460 | missense variant | G/T | snv | 8.3E-02 | 8.3E-02 | 0.010 | < 0.001 | 1 | 2019 | 2019 | |||||
|
2 | X | 133027131 | missense variant | G/A;T | snv | 3.8E-02 | 0.010 | < 0.001 | 1 | 2008 | 2008 | ||||||
|
2 | 1.000 | 0.040 | 2 | 48721568 | 3 prime UTR variant | A/C | snv | 0.29 | 0.010 | < 0.001 | 1 | 2017 | 2017 | ||||
|
38 | 0.627 | 0.600 | 21 | 45531904 | missense variant | C/A;T | snv | 9.7E-06; 1.4E-05 | 0.010 | < 0.001 | 1 | 2010 | 2010 | ||||
|
14 | 0.724 | 0.160 | 2 | 48963902 | missense variant | C/G;T | snv | 4.0E-06; 0.55 | 0.030 | 0.333 | 3 | 2011 | 2015 | ||||
|
17 | 0.708 | 0.240 | 2 | 48962782 | missense variant | C/T | snv | 0.57 | 0.57 | 0.060 | 0.500 | 6 | 2011 | 2017 | |||
|
188 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 0.020 | 0.500 | 2 | 2017 | 2018 | |||
|
226 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.020 | 0.500 | 2 | 2006 | 2012 | |||
|
262 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 0.020 | 0.500 | 2 | 2006 | 2012 | |||
|
174 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 0.020 | 0.500 | 2 | 2013 | 2015 | |||
|
4 | 0.882 | 0.120 | 6 | 32977847 | missense variant | G/A | snv | 0.020 | 0.500 | 2 | 2011 | 2015 | |||||
|
7 | 0.807 | 0.040 | 1 | 2461209 | intron variant | G/C | snv | 0.64 | 0.020 | 0.500 | 2 | 2014 | 2019 | ||||
|
205 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 0.020 | 0.500 | 2 | 2017 | 2018 | |||
|
101 | 0.531 | 0.840 | 5 | 7870860 | missense variant | A/G | snv | 0.47 | 0.45 | 0.060 | 0.667 | 6 | 2014 | 2019 | |||
|
306 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.688 | 16 | 2005 | 2019 | |||||
|
34 | 0.653 | 0.600 | 7 | 17339486 | missense variant | G/A | snv | 0.15 | 0.22 | 0.040 | 0.750 | 4 | 2004 | 2019 | |||
|
246 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 0.060 | 0.833 | 6 | 2008 | 2017 | ||||
|
135 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 0.060 | 0.833 | 6 | 2006 | 2017 |