HLA-DPB1, major histocompatibility complex, class II, DP beta 1, 3115
N. diseases: 324; N. variants: 114
Source: ALL
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.724 | 0.440 | 6 | 33087084 | 3 prime UTR variant | A/G | snv | 0.25 |
|
Digestive System Diseases; Infections | 0.900 | 0.917 | 24 | 2009 | 2018 | |||||||
|
0.851 | 0.160 | 6 | 33075103 | intron variant | A/G | snv | 0.19 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.810 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.790 | 0.520 | 6 | 33087761 | 3 prime UTR variant | C/T | snv | 0.38 |
|
Respiratory Tract Diseases; Immune System Diseases; Cardiovascular Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.851 | 0.160 | 6 | 33075103 | intron variant | A/G | snv | 0.19 |
|
Skin and Connective Tissue Diseases | 0.800 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.724 | 0.440 | 6 | 33087084 | 3 prime UTR variant | A/G | snv | 0.25 |
|
Digestive System Diseases; Infections | 0.760 | 1.000 | 8 | 2011 | 2017 | |||||||
|
0.724 | 0.440 | 6 | 33087084 | 3 prime UTR variant | A/G | snv | 0.25 |
|
Digestive System Diseases; Neoplasms | 0.740 | 0.800 | 5 | 2012 | 2015 | |||||||
|
0.724 | 0.440 | 6 | 33087084 | 3 prime UTR variant | A/G | snv | 0.25 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications | 0.720 | 1.000 | 3 | 2013 | 2018 | |||||||
|
1.000 | 0.080 | 6 | 33080909 | missense variant | G/A;T | snv | 0.31; 1.4E-02 |
|
Digestive System Diseases; Infections | 0.710 | 1.000 | 3 | 2013 | 2019 | |||||||
|
0.925 | 0.080 | 6 | 33077781 | intron variant | G/A | snv | 0.32 |
|
Digestive System Diseases; Infections | 0.710 | 0.667 | 3 | 2009 | 2016 | |||||||
|
0.724 | 0.440 | 6 | 33087084 | 3 prime UTR variant | A/G | snv | 0.25 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.710 | 1.000 | 3 | 2007 | 2018 | |||||||
|
0.851 | 0.280 | 6 | 33087470 | 3 prime UTR variant | T/A;C | snv |
|
Digestive System Diseases; Infections | 0.710 | 1.000 | 3 | 2012 | 2016 | ||||||||
|
0.925 | 0.160 | 6 | 33081144 | non coding transcript exon variant | A/G | snv | 0.27 |
|
Digestive System Diseases; Infections | 0.710 | 1.000 | 2 | 2013 | 2015 | |||||||
|
0.827 | 0.320 | 6 | 33082502 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases; Infections | 0.710 | 1.000 | 2 | 2013 | 2013 | |||||||
|
1.000 | 0.080 | 6 | 33085905 | missense variant | G/A;C | snv | 0.32; 4.1E-06 |
|
Digestive System Diseases; Infections | 0.710 | 1.000 | 2 | 2013 | 2016 | |||||||
|
0.790 | 0.280 | 6 | 33087030 | 3 prime UTR variant | A/G | snv | 0.38 |
|
Digestive System Diseases; Infections | 0.710 | 0.500 | 2 | 2013 | 2018 | |||||||
|
0.882 | 0.280 | 6 | 33088122 | 3 prime UTR variant | G/A | snv | 0.14 |
|
Skin and Connective Tissue Diseases | 0.710 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.925 | 0.120 | 6 | 33077921 | intron variant | G/A | snv | 9.5E-02 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases | 0.710 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.790 | 0.520 | 6 | 33087761 | 3 prime UTR variant | C/T | snv | 0.38 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 3 | 2007 | 2011 | |||||||
|
0.925 | 0.200 | 6 | 33079254 | intron variant | T/C | snv | 0.37 |
|
Digestive System Diseases; Infections | 0.700 | 1.000 | 2 | 2012 | 2013 | |||||||
|
1.000 | 0.080 | 6 | 33080917 | missense variant | A/G | snv |
|
Digestive System Diseases; Infections | 0.700 | 1.000 | 2 | 2013 | 2013 | ||||||||
|
0.790 | 0.520 | 6 | 33087761 | 3 prime UTR variant | C/T | snv | 0.38 |
|
Digestive System Diseases; Infections | 0.700 | 1.000 | 2 | 2011 | 2013 | |||||||
|
0.851 | 0.160 | 6 | 33075103 | intron variant | A/G | snv | 0.19 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2007 | 2009 | |||||||
|
6 | 33080829 | missense variant | G/C | snv | 0.14 | 0.15 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
6 | 33080829 | missense variant | G/C | snv | 0.14 | 0.15 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.925 | 0.240 | 6 | 33080884 | missense variant | A/G | snv | 0.18 | 0.25 |
|
Respiratory Tract Diseases; Immune System Diseases; Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2013 | 2013 |