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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
490 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 0.030 | 1.000 | 3 | 2012 | 2019 | ||||
|
614 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 0.030 | 1.000 | 3 | 2004 | 2019 | |||
|
480 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.030 | 1.000 | 3 | 2012 | 2019 | |||||
|
3 | 0.925 | 0.120 | 6 | 33579060 | intron variant | T/C | snv | 0.74 | 0.820 | 1.000 | 3 | 2012 | 2013 | ||||
|
4 | 0.851 | 0.280 | 16 | 85942053 | intron variant | C/A;T | snv | 0.820 | 1.000 | 3 | 2010 | 2012 | |||||
|
3 | 0.925 | 0.120 | 11 | 123484683 | intron variant | A/G | snv | 0.15 | 0.710 | 1.000 | 3 | 2016 | 2018 | ||||
|
4 | 0.851 | 0.200 | 2 | 241431686 | missense variant | C/A;T | snv | 4.1E-06; 9.3E-02 | 0.820 | 1.000 | 3 | 2010 | 2013 | ||||
|
2 | 0.925 | 0.120 | 15 | 40111456 | upstream gene variant | C/G | snv | 0.50 | 0.800 | 1.000 | 3 | 2013 | 2017 | ||||
|
5 | 0.827 | 0.240 | 3 | 27736288 | intergenic variant | G/A | snv | 0.59 | 0.700 | 1.000 | 3 | 2016 | 2017 | ||||
|
53 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 0.800 | 1.000 | 2 | 2013 | 2019 | ||||
|
2 | 0.925 | 0.120 | 18 | 50317164 | upstream gene variant | A/G;T | snv | 0.710 | 1.000 | 2 | 2011 | 2017 | |||||
|
2 | 0.925 | 0.120 | 16 | 85922065 | 3 prime UTR variant | C/T | snv | 0.40 | 0.810 | 1.000 | 2 | 2013 | 2014 | ||||
|
3 | 1.000 | 0.120 | 16 | 81912655 | missense variant | C/T | snv | 0.710 | 1.000 | 2 | 2014 | 2015 | |||||
|
1 | 1.000 | 0.120 | 16 | 81928578 | missense variant | A/C;G;T | snv | 0.710 | 1.000 | 2 | 2014 | 2016 | |||||
|
59 | 0.583 | 0.600 | 1 | 114713908 | missense variant | T/A;C;G | snv | 0.710 | 1.000 | 2 | 1997 | 2016 | |||||
|
20 | 0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 2 | 2007 | 2014 | |||||
|
2 | 0.925 | 0.120 | 9 | 22336997 | intergenic variant | G/C;T | snv | 0.800 | 1.000 | 2 | 2013 | 2016 | |||||
|
11 | 0.851 | 0.160 | 22 | 50532837 | upstream gene variant | T/A;C | snv | 0.700 | 1.000 | 2 | 2017 | 2019 | |||||
|
3 | 0.882 | 0.160 | 9 | 22206988 | intron variant | C/A;T | snv | 0.43 | 0.800 | 1.000 | 2 | 2013 | 2017 | ||||
|
2 | 0.925 | 0.120 | 4 | 108105258 | intron variant | A/C;G;T | snv | 0.800 | 1.000 | 2 | 2013 | 2016 | |||||
|
97 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 0.020 | 1.000 | 2 | 2011 | 2011 | ||||
|
6 | 0.827 | 0.160 | 6 | 33579153 | intron variant | T/C | snv | 0.74 | 0.700 | 1.000 | 2 | 2017 | 2017 | ||||
|
5 | 0.827 | 0.280 | 8 | 127180736 | intron variant | A/G | snv | 0.30 | 0.720 | 1.000 | 2 | 2010 | 2010 | ||||
|
2 | 0.925 | 0.120 | 8 | 102566646 | regulatory region variant | T/G | snv | 0.41 | 0.800 | 1.000 | 2 | 2013 | 2016 | ||||
|
2 | 0.925 | 0.120 | 11 | 2299865 | intron variant | C/A;T | snv | 0.800 | 1.000 | 2 | 2013 | 2016 |