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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
17 | 78860884 | intron variant | G/A;C | snv |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
17 | 78894782 | intron variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
17 | 78897589 | non coding transcript exon variant | A/G | snv | 0.28 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.120 | 17 | 78897053 | intron variant | C/T | snv | 0.14 |
|
Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
17 | 78898598 | non coding transcript exon variant | A/G | snv | 0.97 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
0.925 | 0.120 | 17 | 78885621 | intron variant | T/A;C | snv |
|
Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.120 | 17 | 78885621 | intron variant | T/A;C | snv |
|
Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
17 | 78906167 | intron variant | T/C | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 17 | 78877679 | intron variant | T/C | snv | 0.17 |
|
Musculoskeletal Diseases | 0.010 | < 0.001 | 1 | 2019 | 2019 | |||||||
|
0.807 | 0.320 | 17 | 78870935 | synonymous variant | C/T | snv | 0.13 | 0.11 |
|
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.807 | 0.320 | 17 | 78870935 | synonymous variant | C/T | snv | 0.13 | 0.11 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.807 | 0.320 | 17 | 78870935 | synonymous variant | C/T | snv | 0.13 | 0.11 |
|
Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
0.807 | 0.320 | 17 | 78870935 | synonymous variant | C/T | snv | 0.13 | 0.11 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
0.807 | 0.320 | 17 | 78870935 | synonymous variant | C/T | snv | 0.13 | 0.11 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.807 | 0.320 | 17 | 78870935 | synonymous variant | C/T | snv | 0.13 | 0.11 |
|
Female Urogenital Diseases and Pregnancy Complications | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1.000 | 0.040 | 17 | 78870629 | intron variant | C/A;G;T | snv |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.040 | 17 | 78874211 | intron variant | A/G | snv | 0.93 |
|
Musculoskeletal Diseases | 0.010 | < 0.001 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 17 | 78915454 | intron variant | G/A;T | snv |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 0.120 | 17 | 78901892 | 5 prime UTR variant | C/T | snv | 0.52 |
|
Nervous System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.882 | 0.120 | 17 | 78901892 | 5 prime UTR variant | C/T | snv | 0.52 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.882 | 0.120 | 17 | 78901892 | 5 prime UTR variant | C/T | snv | 0.52 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.882 | 0.120 | 17 | 78901892 | 5 prime UTR variant | C/T | snv | 0.52 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 17 | 78871011 | splice region variant | A/G | snv | 1.2E-05 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 17 | 78855681 | missense variant | T/C;G | snv | 4.0E-06; 7.2E-05 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 17 | 78878430 | intron variant | A/C;G;T | snv |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 |