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rs7100749

From SNPedia

Orientationplus
Stabilizedplus
Make rs7100749(C;C)
Make rs7100749(C;T)
Make rs7100749(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position52772139
GeneMBL2
is asnp
is mentioned by
dbSNPrs7100749
dbSNP (classic)rs7100749
ClinGenrs7100749
ebirs7100749
HLIrs7100749
Exacrs7100749
Gnomadrs7100749
Varsomers7100749
LitVarrs7100749
Maprs7100749
PheGenIrs7100749
Biobankrs7100749
1000 genomesrs7100749
hgdprs7100749
ensemblrs7100749
geneviewrs7100749
scholarrs7100749
googlers7100749
pharmgkbrs7100749
gwascentralrs7100749
openSNPrs7100749
23andMers7100749
SNPshotrs7100749
SNPdbers7100749
MSV3drs7100749
GWAS Ctlgrs7100749
GMAF0.04454
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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


[PMID 20465856OA-icon.png] Phylogenetic nomenclature and evolution of mannose-binding lectin (MBL2) haplotypes.