rs7096206
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| Make rs7096206(C;G) |
| Make rs7096206(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 52771925 |
| Gene | MBL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7096206 |
| dbSNP (classic) | rs7096206 |
| ClinGen | rs7096206 |
| ebi | rs7096206 |
| HLI | rs7096206 |
| Exac | rs7096206 |
| Gnomad | rs7096206 |
| Varsome | rs7096206 |
| LitVar | rs7096206 |
| Map | rs7096206 |
| PheGenI | rs7096206 |
| Biobank | rs7096206 |
| 1000 genomes | rs7096206 |
| hgdp | rs7096206 |
| ensembl | rs7096206 |
| geneview | rs7096206 |
| scholar | rs7096206 |
| rs7096206 | |
| pharmgkb | rs7096206 |
| gwascentral | rs7096206 |
| openSNP | rs7096206 |
| 23andMe | rs7096206 |
| SNPshot | rs7096206 |
| SNPdbe | rs7096206 |
| MSV3d | rs7096206 |
| GWAS Ctlg | rs7096206 |
| GMAF | 0.1832 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22994203] MBL2 gene variation affecting serum MBL is associated with prosthetic joint infection in Czech patients after total joint arthroplasty
[PMID 23423485] Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China
[PMID 17898783] Association of polymorphisms in the mannose-binding lectin gene and pulmonary morbidity in preterm infants.
[PMID 17942372] Association between early onset and organ manifestations of systemic lupus erythematosus (SLE) and a down-regulating promoter polymorphism in the MBL2 gene.
[PMID 18396467
] Genetic variation and haplotype structures of innate immunity genes in eastern India.
[PMID 18452612] MBL2 and hepatitis C virus infection among injection drug users.
[PMID 18936436] Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.
[PMID 19139195] Genetic polymorphisms of mannose-binding lectin do not influence placental malaria but are associated with preterm deliveries.
[PMID 19366862] Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy.
[PMID 19432958] Haplotype specific-sequencing reveals MBL2 association with asymptomatic Plasmodium falciparum infection.
[PMID 20042521] Genotypes coding for low serum levels of mannose-binding lectin are underrepresented among individuals suffering from noninfectious systemic inflammatory response syndrome.
[PMID 20463618] Role of polymorphic variants as genetic modulators of infection in neonatal sepsis.
[PMID 20465856] Phylogenetic nomenclature and evolution of mannose-binding lectin (MBL2) haplotypes.
[PMID 21211797] Mannose binding lectin 2 haplotypes do not affect the progression of coronary atherosclerosis in men with proven coronary artery disease treated with pravastatin.
[PMID 21733090] Association of mannose-binding lectin-2 gene polymorphism with the development of hepatitis C-induced hepatocellular carcinoma.
[PMID 22650645] Role of mannose-binding lectin-2 polymorphism in the development of acute cellular rejection after transplantation for hepatitis C virus-induced liver disease.
[PMID 22848725] Mannose-binding lectin deficiency is associated with myocardial infarction: the HUNT2 study in Norway.
[PMID 23107763] Host genetic risk factors for community-acquired pneumonia.
[PMID 23662819] Complement polymorphisms and cognitive dysfunction after carotid endarterectomy.
[PMID 24952212] Age-dependent Association of Mannose-Binding Lectin Polymorphisms with the Development of Pulmonary Tuberculosis in Viet Nam
[PMID 25787238] Impact of Mannose-Binding Lectin 2 Polymorphism on the Risk of Hepatocellular Carcinoma: A Case-Control Study in Chinese Han Population
