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 | 5 | 1341708 | missense variant | T/C | snv | 2.1E-05 | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||
|
2 | 1.000 | 0.040 | 7 | 129203401 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||
|
2 | 1.000 | 0.040 | 9 | 95479023 | missense variant | C/T | snv | 2.1E-05 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 1.000 | 0.040 | 19 | 45395856 | missense variant | T/C | snv | 0.010 | < 0.001 | 1 | 2005 | 2005 | |||||
|
2 | 0.925 | 0.040 | 7 | 129210997 | missense variant | G/A | snv | 4.0E-05 | 2.8E-05 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.040 | 5 | 87349304 | missense variant | G/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.040 | 5 | 87349309 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.040 | 5 | 87349312 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.080 | 6 | 471136 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||
|
8 | 0.827 | 0.080 | 16 | 89919436 | missense variant | G/T | snv | 8.6E-02 | 8.0E-02 | 0.010 | 1.000 | 1 | 2006 | 2006 | |||
|
3 | 0.925 | 0.080 | 10 | 49470323 | missense variant | T/C | snv | 0.22 | 0.20 | 0.010 | 1.000 | 1 | 2012 | 2012 | |||
|
4 | 0.925 | 0.080 | 10 | 49459059 | missense variant | T/C | snv | 0.22 | 0.19 | 0.010 | 1.000 | 1 | 2012 | 2012 | |||
|
4 | 0.851 | 0.080 | 7 | 129210500 | missense variant | G/T | snv | 0.700 | 0 | ||||||||
|
6 | 0.807 | 0.120 | 1 | 17395867 | intron variant | G/A | snv | 0.37 | 0.700 | 1.000 | 2 | 2008 | 2014 | ||||
|
5 | 0.827 | 0.120 | 1 | 228862088 | downstream gene variant | T/G | snv | 0.48 | 0.700 | 1.000 | 2 | 2008 | 2014 | ||||
|
3 | 0.925 | 0.120 | 7 | 155806527 | missense variant | T/A | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||
|
6 | 0.827 | 0.120 | 12 | 52519884 | missense variant | C/T | snv | 5.7E-02 | 5.3E-02 | 0.010 | 1.000 | 1 | 2009 | 2009 | |||
|
8 | 0.790 | 0.120 | 2 | 47403074 | 5 prime UTR variant | T/C | snv | 0.10 | 0.010 | < 0.001 | 1 | 2018 | 2018 | ||||
|
5 | 0.851 | 0.120 | 11 | 108229185 | stop gained | C/G;T | snv | 8.1E-06 | 0.700 | 0 | |||||||
|
6 | 0.827 | 0.160 | 9 | 95447156 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | |||||
|
4 | 0.882 | 0.160 | 7 | 155806509 | missense variant | A/C;G | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||
|
14 | 0.732 | 0.160 | 17 | 7674089 | intron variant | A/C | snv | 0.10 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
5 | 0.925 | 0.160 | 12 | 57470802 | stop gained | C/T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
|
6 | 0.827 | 0.160 | 9 | 95447312 | missense variant | G/A;C;T | snv | 0.39; 1.2E-05; 4.1E-06 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
|
13 | 0.776 | 0.200 | 5 | 33951588 | missense variant | C/A;G | snv | 0.65 | 0.010 | 1.000 | 1 | 2009 | 2009 |