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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
16 | 0.716 | 0.240 | 10 | 122454932 | missense variant | G/T | snv | 0.26 | 0.23 | 0.100 | 0.923 | 26 | 2007 | 2019 | |||
|
14 | 0.724 | 0.280 | 10 | 122461028 | non coding transcript exon variant | G/A | snv | 0.23 | 0.100 | 0.900 | 10 | 2007 | 2016 | ||||
|
33 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 0.100 | 1.000 | 12 | 2008 | 2017 | |||
|
72 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 0.060 | 0.833 | 6 | 2008 | 2013 | |||
|
5 | 0.882 | 0.040 | 1 | 196651787 | upstream gene variant | C/T | snv | 0.22 | 0.020 | 1.000 | 2 | 2008 | 2009 | ||||
|
3 | 0.882 | 0.160 | 6 | 31943161 | intron variant | G/T | snv | 0.12 | 0.050 | 1.000 | 5 | 2009 | 2015 | ||||
|
8 | 0.790 | 0.280 | 17 | 1769982 | missense variant | C/T | snv | 0.61 | 0.69 | 0.020 | 1.000 | 2 | 2009 | 2012 | |||
|
9 | 0.790 | 0.320 | 6 | 31946247 | missense variant | T/A | snv | 3.9E-02 | 3.4E-02 | 0.020 | 1.000 | 2 | 2009 | 2014 | |||
|
131 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 0.010 | < 0.001 | 1 | 2009 | 2009 | |||
|
7 | 0.790 | 0.160 | 6 | 31946403 | missense variant | G/A;T | snv | 9.6E-02; 4.1E-06 | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||
|
10 | 0.763 | 0.360 | 6 | 31936027 | missense variant | G/A;C | snv | 4.1E-06; 3.9E-02 | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.882 | 0.160 | 11 | 57610852 | intron variant | C/T | snv | 0.39 | 0.030 | < 0.001 | 3 | 2010 | 2015 | ||||
|
11 | 0.807 | 0.240 | 1 | 196727803 | intron variant | G/A | snv | 0.46 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
3 | 0.882 | 0.040 | 10 | 122459759 | non coding transcript exon variant | C/G | snv | 0.23 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
3 | 0.882 | 0.160 | 7 | 74037810 | non coding transcript exon variant | G/A | snv | 0.11 | 0.020 | 0.500 | 2 | 2011 | 2011 | ||||
|
14 | 0.732 | 0.320 | 15 | 73927205 | missense variant | G/T | snv | 0.33 | 0.28 | 0.010 | 1.000 | 1 | 2011 | 2011 | |||
|
44 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
51 | 0.602 | 0.640 | 4 | 186082920 | missense variant | C/G;T | snv | 1.2E-04; 0.28 | 0.010 | < 0.001 | 1 | 2011 | 2011 | ||||
|
5 | 0.851 | 0.200 | 6 | 43774842 | non coding transcript exon variant | T/C;G | snv | 0.020 | 1.000 | 2 | 2012 | 2015 | |||||
|
2 | 0.925 | 0.040 | 6 | 31933645 | missense variant | G/A;T | snv | 2.0E-05; 1.6E-05 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
4 | 0.882 | 0.040 | 4 | 56920284 | intron variant | G/T | snv | 0.92 | 0.010 | < 0.001 | 1 | 2012 | 2012 | ||||
|
2 | 0.925 | 0.040 | 7 | 80656534 | splice region variant | T/C | snv | 0.14 | 0.13 | 0.010 | 1.000 | 1 | 2012 | 2012 | |||
|
2 | 0.925 | 0.040 | 7 | 80660605 | intron variant | A/T | snv | 0.29 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
6 | 0.827 | 0.160 | 7 | 94413927 | missense variant | C/A;G;T | snv | 8.0E-06; 0.77; 8.0E-06 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
3 | 0.882 | 0.160 | 6 | 31949174 | non coding transcript exon variant | T/C | snv | 0.12 | 0.010 | 1.000 | 1 | 2012 | 2012 |