{{Rsnum
|rsid=7851696
|Gene=FCN2
|Chromosome=9
|position=134887245
|Orientation=plus
|GMAF=0.1492
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=FCN2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 75.2 | 24.8 | 0.0
| HCB | 62.8 | 33.6 | 3.6
| JPT | 73.5 | 26.5 | 0.0
| YRI | 63.3 | 34.7 | 2.0
| ASW | 56.1 | 38.6 | 5.3
| CHB | 62.8 | 33.6 | 3.6
| CHD | 73.4 | 25.7 | 0.9
| GIH | 86.1 | 12.9 | 1.0
| LWK | 68.8 | 25.7 | 5.5
| MEX | 72.4 | 25.9 | 1.7
| MKK | 51.9 | 41.7 | 6.4
| TSI | 85.3 | 13.7 | 1.0
| HapMapRevision=28
}}{{omim
|desc=FICOLIN 2; FCN2
|id=601624
|rsnum=7851696
}}

{{PMID Auto
|PMID=17680820
|Title=Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 gene.
|OA=1
}}

{{PMID Auto
|PMID=19220833
|Title=Exploring the role of polymorphisms in ficolin genes in respiratory tract infections in children.
|OA=1
}}

{{GET Evidence
|gene=FCN2
|aa_change=Ala258Ser
|aa_change_short=A258S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7851696
|overall_frequency_n=1461
|overall_frequency_d=10758
|overall_frequency=0.135806
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.826
|nblosum100=-1
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=23423485
|Title=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 Auto
|PMID=22848725
|Title=Mannose-binding lectin deficiency is associated with myocardial infarction: the HUNT2 study in Norway.
|OA=1
}}

{{PMID Auto
|PMID=22892990
|Title=The functional polymorphism Ala258Ser in the innate receptor gene ficolin-2 in the donor predicts improved renal transplant outcome.
}}

{{PMID Auto
|PMID=22940091
|Title=Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients.
}}

{{PMID Auto
|PMID=23525825
|Title=Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}