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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 169165889 | intron variant | A/C | snv | 5.5E-02 |
|
Cardiovascular Diseases | 0.800 | 1.000 | 2 | 2011 | 2012 | |||||||||
|
1 | 169133102 | intron variant | T/A | snv | 9.9E-02 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||||
|
1 | 169327626 | intron variant | C/G;T | snv |
|
Cardiovascular Diseases | 0.700 | 1.000 | 2 | 2011 | 2012 | ||||||||||
|
1 | 169303213 | non coding transcript exon variant | A/C;T | snv | 0.96 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1 | 169303215 | non coding transcript exon variant | G/A;T | snv | 0.96 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1 | 169132697 | 3 prime UTR variant | C/G;T | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1 | 169345192 | intron variant | T/C | snv | 0.95 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1 | 169327626 | intron variant | C/G;T | snv |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 169355555 | intron variant | T/C;G | snv |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 169355555 | intron variant | T/C;G | snv |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 1 | 169183350 | intron variant | C/T | snv | 0.24 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 169191220 | intron variant | C/T | snv | 1.7E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1 | 169165889 | intron variant | A/C | snv | 5.5E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1 | 169247174 | intron variant | C/G;T | snv |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 169140155 | intron variant | G/A | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1 | 169238941 | intron variant | C/T | snv | 0.98 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1 | 169145784 | intron variant | T/C | snv | 3.4E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 |