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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2018 | 2019 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2018 | 2019 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Endocrine System Diseases | 0.020 | 1.000 | 2 | 2014 | 2017 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2018 | 2019 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Infections; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2018 | 2019 | |||||||
|
0.851 | 0.120 | 19 | 51692221 | intron variant | G/A;C | snv | 0.30 |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2016 | 2017 | |||||||
|
0.851 | 0.120 | 19 | 51692221 | intron variant | G/A;C | snv | 0.30 |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2016 | 2017 | |||||||
|
1.000 | 0.040 | 19 | 51693235 | non coding transcript exon variant | G/A;C | snv | 2.6E-03; 5.5E-06 |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Eye Diseases; Immune System Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Endocrine System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2020 | 2020 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2020 | 2020 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 |
|
Nervous System Diseases; Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.851 | 0.120 | 19 | 51692221 | intron variant | G/A;C | snv | 0.30 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.851 | 0.120 | 19 | 51692221 | intron variant | G/A;C | snv | 0.30 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 |