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rs10824792

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs10824792(C;T)
Make rs10824792(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position52766446
GeneLOC105378305, MBL2
is asnp
is mentioned by
dbSNPrs10824792
dbSNP (classic)rs10824792
ClinGenrs10824792
ebirs10824792
HLIrs10824792
Exacrs10824792
Gnomadrs10824792
Varsomers10824792
LitVarrs10824792
Maprs10824792
PheGenIrs10824792
Biobankrs10824792
1000 genomesrs10824792
hgdprs10824792
ensemblrs10824792
geneviewrs10824792
scholarrs10824792
googlers10824792
pharmgkbrs10824792
gwascentralrs10824792
openSNPrs10824792
23andMers10824792
SNPshotrs10824792
SNPdbers10824792
MSV3drs10824792
GWAS Ctlgrs10824792
GMAF0.4848
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 23576520OA-icon.png] Genetic Polymorphisms in Host Innate Immune Sensor Genes and the Risk of Nasopharyngeal Carcinoma in North Africa


[PMID 17071626] The mannose-binding lectin (MBL2) haplotype and breast cancer: an association study in African-American and Caucasian women.


[PMID 17327408OA-icon.png] Prognostic significance of host immune gene polymorphisms in follicular lymphoma survival.


[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 18633131OA-icon.png] Host immune gene polymorphisms in combination with clinical and demographic factors predict late survival in diffuse large B-cell lymphoma patients in the pre-rituximab era.


[PMID 20056178] Polymorphisms in innate immunity genes and patients response to dendritic cell-based HIV immuno-treatment.


ClinVar
Risk rs10824792(T;T)
Alt rs10824792(T;T)
Reference Rs10824792(C;C)
Significance Probable-non-pathogenic
Disease Mannose-binding protein deficiency
Variation info
Gene MBL2
CLNDBN Mannose-binding protein deficiency
Reversed 0
HGVS NC_000010.10:g.54526206C>T
CLNSRC
CLNACC RCV000277266.1,



[PMID 30482481] SNPs in 3'-UTR region of MBL2 increases susceptibility to recurrent vulvovaginal infections by altering sMBL levels.


[PMID 31080578OA-icon.png] Impact of SNPs interplay across the locus of MBL2, between MBL and Dectin-1 gene, on women's risk of developing recurrent vulvovaginal infections.