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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 160704599 | intron variant | T/C | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160742498 | intron variant | T/G | snv | 2.4E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160714170 | intron variant | C/T | snv | 9.3E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
6 | 160716631 | intron variant | T/G | snv | 0.21 | 0.23 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
6 | 160731873 | missense variant | C/T | snv | 6.6E-03 | 7.6E-03 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
6 | 160752696 | intron variant | C/G | snv | 1.0E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160734232 | intron variant | T/C | snv | 6.4E-03 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
6 | 160707981 | non coding transcript exon variant | G/A | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160704387 | intron variant | T/C | snv | 0.38 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.040 | 6 | 160702419 | intron variant | T/C | snv | 5.7E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 6 | 160702419 | intron variant | T/C | snv | 5.7E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | 6 | 160739148 | missense variant | A/G | snv | 4.0E-06 |
|
Female Urogenital Diseases and Pregnancy Complications | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.040 | 6 | 160716958 | intron variant | G/A | snv | 0.39 |
|
Endocrine System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.040 | 6 | 160716958 | intron variant | G/A | snv | 0.39 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.827 | 0.080 | 6 | 160722576 | intron variant | T/C;G | snv | 0.21 |
|
Cardiovascular Diseases | 0.710 | 1.000 | 2 | 2013 | 2015 | |||||||
|
0.827 | 0.080 | 6 | 160722576 | intron variant | T/C;G | snv | 0.21 |
|
Stomatognathic Diseases | 0.020 | 0.500 | 2 | 2015 | 2017 | |||||||
|
0.827 | 0.080 | 6 | 160722576 | intron variant | T/C;G | snv | 0.21 |
|
Stomatognathic Diseases | 0.020 | 0.500 | 2 | 2015 | 2017 | |||||||
|
0.827 | 0.080 | 6 | 160722576 | intron variant | T/C;G | snv | 0.21 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.827 | 0.080 | 6 | 160722576 | intron variant | T/C;G | snv | 0.21 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.080 | 6 | 160731092 | missense variant | A/C | snv | 4.0E-06 |
|
Female Urogenital Diseases and Pregnancy Complications | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.080 | 6 | 160731092 | missense variant | A/C | snv | 4.0E-06 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.080 | 6 | 160731092 | missense variant | A/C | snv | 4.0E-06 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.080 | 6 | 160718329 | missense variant | T/C | snv | 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.010 | 1.000 | 1 | 2000 | 2000 | |||||||
|
1.000 | 0.080 | 6 | 160706424 | missense variant | G/A | snv | 8.0E-06 |
|
Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.882 | 0.080 | 6 | 160718313 | synonymous variant | T/C | snv | 1.2E-05 | 7.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2003 | 2003 |