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rs7096206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
Make rs7096206(C;G)
Make rs7096206(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position52771925
GeneMBL2
is asnp
is mentioned by
dbSNPrs7096206
dbSNP (classic)rs7096206
ClinGenrs7096206
ebirs7096206
HLIrs7096206
Exacrs7096206
Gnomadrs7096206
Varsomers7096206
LitVarrs7096206
Maprs7096206
PheGenIrs7096206
Biobankrs7096206
1000 genomesrs7096206
hgdprs7096206
ensemblrs7096206
geneviewrs7096206
scholarrs7096206
googlers7096206
pharmgkbrs7096206
gwascentralrs7096206
openSNPrs7096206
23andMers7096206
SNPshotrs7096206
SNPdbers7096206
MSV3drs7096206
GWAS Ctlgrs7096206
GMAF0.1832
Max Magnitude0
? (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 18396467OA-icon.png] Genetic variation and haplotype structures of innate immunity genes in eastern India.


[PMID 18452612OA-icon.png] MBL2 and hepatitis C virus infection among injection drug users.


[PMID 18936436OA-icon.png] Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.


[PMID 19139195OA-icon.png] Genetic polymorphisms of mannose-binding lectin do not influence placental malaria but are associated with preterm deliveries.


[PMID 19366862OA-icon.png] Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy.


[PMID 19432958OA-icon.png] Haplotype specific-sequencing reveals MBL2 association with asymptomatic Plasmodium falciparum infection.


[PMID 20042521OA-icon.png] Genotypes coding for low serum levels of mannose-binding lectin are underrepresented among individuals suffering from noninfectious systemic inflammatory response syndrome.


[PMID 20463618OA-icon.png] Role of polymorphic variants as genetic modulators of infection in neonatal sepsis.


[PMID 20465856OA-icon.png] 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 22848725OA-icon.png] 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 23662819OA-icon.png] 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 25787238OA-icon.png] Impact of Mannose-Binding Lectin 2 Polymorphism on the Risk of Hepatocellular Carcinoma: A Case-Control Study in Chinese Han Population