Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.790 | 0.120 | 19 | 55154146 | missense variant | G/A;C | snv | 4.0E-06 |
|
Cardiovascular Diseases | 0.810 | 1.000 | 2 | 2003 | 2016 | |||||||
|
0.827 | 0.080 | 19 | 55151892 | missense variant | C/A;G;T | snv |
|
Cardiovascular Diseases | 0.810 | 1.000 | 2 | 2003 | 2010 | ||||||||
|
1.000 | 0.040 | 19 | 55154047 | missense variant | T/C | snv |
|
Cardiovascular Diseases | 0.810 | 1.000 | 2 | 2003 | 2005 | ||||||||
|
0.925 | 0.040 | 19 | 55154148 | missense variant | A/G;T | snv |
|
Cardiovascular Diseases | 0.810 | 1.000 | 2 | 2003 | 2016 | ||||||||
|
0.790 | 0.120 | 19 | 55154094 | missense variant | C/A;G;T | snv | 4.0E-05 |
|
0.800 | 1.000 | 10 | 1997 | 2012 | ||||||||
|
0.790 | 0.120 | 19 | 55154146 | missense variant | G/A;C | snv | 4.0E-06 |
|
0.800 | 1.000 | 9 | 1997 | 2017 | ||||||||
|
0.882 | 0.080 | 19 | 55151851 | missense variant | T/C;G | snv |
|
0.800 | 1.000 | 9 | 1997 | 2017 | |||||||||
|
0.882 | 0.080 | 19 | 55151881 | missense variant | C/A;T | snv | 4.0E-06 |
|
0.800 | 1.000 | 9 | 1997 | 2017 | ||||||||
|
0.882 | 0.080 | 19 | 55154109 | missense variant | G/A | snv |
|
0.800 | 1.000 | 9 | 1997 | 2017 | |||||||||
|
0.925 | 0.080 | 19 | 55154082 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 |
|
0.800 | 1.000 | 4 | 2011 | 2017 | |||||||
|
0.925 | 0.040 | 19 | 55151912 | missense variant | G/C | snv |
|
Cardiovascular Diseases | 0.800 | 1.000 | 2 | 2009 | 2012 | ||||||||
|
0.925 | 0.040 | 19 | 55157052 | missense variant | T/G | snv |
|
Cardiovascular Diseases | 0.800 | 1.000 | 2 | 2009 | 2012 | ||||||||
|
0.790 | 0.120 | 19 | 55154146 | missense variant | G/A;C | snv | 4.0E-06 |
|
Cardiovascular Diseases | 0.740 | 1.000 | 30 | 1997 | 2016 | |||||||
|
0.790 | 0.120 | 19 | 55154146 | missense variant | G/A;C | snv | 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.730 | 1.000 | 17 | 1997 | 2017 | |||||||
|
0.851 | 0.120 | 19 | 55154095 | missense variant | G/A | snv | 4.0E-05 | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.720 | 1.000 | 15 | 1997 | 2017 | ||||||
|
0.827 | 0.080 | 19 | 55151892 | missense variant | C/A;G;T | snv |
|
Cardiovascular Diseases | 0.710 | 1.000 | 13 | 2003 | 2013 | ||||||||
|
0.827 | 0.080 | 19 | 55151892 | missense variant | C/A;G;T | snv |
|
Cardiovascular Diseases | 0.710 | 1.000 | 11 | 2003 | 2013 | ||||||||
|
0.851 | 0.120 | 19 | 55151910 | missense variant | C/T | snv | 7.0E-06 |
|
Cardiovascular Diseases | 0.710 | 0.909 | 11 | 2003 | 2017 | |||||||
|
0.827 | 0.120 | 19 | 55154070 | missense variant | C/T | snv |
|
Cardiovascular Diseases | 0.710 | 1.000 | 3 | 2007 | 2016 | ||||||||
|
0.790 | 0.120 | 19 | 55154094 | missense variant | C/A;G;T | snv | 4.0E-05 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 22 | 1997 | 2017 | |||||||
|
0.790 | 0.120 | 19 | 55154094 | missense variant | C/A;G;T | snv | 4.0E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 1.000 | 17 | 1997 | 2017 | |||||||
|
0.882 | 0.080 | 19 | 55154109 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 1.000 | 12 | 2003 | 2017 | ||||||||
|
0.851 | 0.120 | 19 | 55154157 | missense variant | C/T | snv | 4.2E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 1.000 | 11 | 2003 | 2017 | |||||||
|
0.851 | 0.120 | 19 | 55154157 | missense variant | C/T | snv | 4.2E-05 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 11 | 2003 | 2014 | |||||||
|
0.827 | 0.080 | 19 | 55151892 | missense variant | C/A;G;T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 1.000 | 10 | 2003 | 2015 |