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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 16 | 3963466 | 3 prime UTR variant | C/T | snv | 0.45 |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.040 | 16 | 4053870 | intron variant | T/C | snv | 0.77 |
|
Nervous System Diseases | 0.800 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.925 | 0.080 | 16 | 4015582 | non coding transcript exon variant | A/G | snv | 0.51 |
|
Cardiovascular Diseases | 0.710 | 1.000 | 2 | 2015 | 2017 | |||||||
|
1.000 | 0.080 | 16 | 3963466 | 3 prime UTR variant | C/T | snv | 0.45 |
|
0.700 | 1.000 | 5 | 2014 | 2019 | ||||||||
|
16 | 3965728 | 3 prime UTR variant | C/T | snv | 0.49 | 0.46 |
|
0.700 | 1.000 | 2 | 2017 | 2018 | |||||||||
|
16 | 4078852 | intron variant | G/C | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
16 | 3965312 | 3 prime UTR variant | A/G | snv | 0.67 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.080 | 16 | 4056787 | intron variant | C/A;T | snv |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
16 | 4087261 | intron variant | A/G | snv | 0.20 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
16 | 4070075 | intron variant | G/A | snv | 0.59 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
16 | 3964281 | 3 prime UTR variant | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
16 | 3988386 | intron variant | G/A | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
16 | 3988386 | intron variant | G/A | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
16 | 3988386 | intron variant | G/A | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
16 | 3971733 | intron variant | A/G | snv | 0.80 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
16 | 3971733 | intron variant | A/G | snv | 0.80 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
1.000 | 0.080 | 16 | 3963466 | 3 prime UTR variant | C/T | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 16 | 3963466 | 3 prime UTR variant | C/T | snv | 0.45 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.080 | 16 | 3963466 | 3 prime UTR variant | C/T | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 16 | 3963466 | 3 prime UTR variant | C/T | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 16 | 3963466 | 3 prime UTR variant | C/T | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
16 | 3972693 | intron variant | C/T | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
16 | 3985067 | intron variant | A/G | snv | 0.59 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
16 | 3969349 | intron variant | C/T | snv | 0.66 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
16 | 3979970 | intron variant | -/CT | delins |
|
0.700 | 1.000 | 1 | 2019 | 2019 |