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rs7851696

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs7851696(G;T)
Make rs7851696(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position134887245
GeneFCN2
is asnp
is mentioned by
dbSNPrs7851696
ebirs7851696
HLIrs7851696
Exacrs7851696
Varsomers7851696
Maprs7851696
PheGenIrs7851696
hapmaprs7851696
1000 genomesrs7851696
hgdprs7851696
ensemblrs7851696
gopubmedrs7851696
geneviewrs7851696
scholarrs7851696
googlers7851696
pharmgkbrs7851696
gwascentralrs7851696
openSNPrs7851696
23andMers7851696
23andMe allrs7851696
SNP Nexus

SNPshotrs7851696
SNPdbers7851696
MSV3drs7851696
GWAS Ctlgrs7851696
GMAF0.1492
Max Magnitude0
? (G;G) (G;T) (T;T) 28
OMIM601624
DescFICOLIN 2; FCN2
Variant
Relatedalso
[PMID 17680820OA-icon.png] Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 gene.


[PMID 19220833OA-icon.png] Exploring the role of polymorphisms in ficolin genes in respiratory tract infections in children.


GET Evidence
FCN2-A258S
aa_change Ala258Ser
aa_change_short A258S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.135806
summary



[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 22848725OA-icon.png] Mannose-binding lectin deficiency is associated with myocardial infarction: the HUNT2 study in Norway.


[PMID 22892990] The functional polymorphism Ala258Ser in the innate receptor gene ficolin-2 in the donor predicts improved renal transplant outcome.


[PMID 22940091] Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients.


[PMID 23525825OA-icon.png] Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.