{{Rsnum
|rsid=17549193
|Gene=FCN2
|Chromosome=9
|position=134887180
|Orientation=plus
|GMAF=0.241
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=FCN2
}}{{omim
|desc=FICOLIN 2; FCN2
|id=601624
|rsnum=17549193
}}

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

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

{{GET Evidence
|gene=FCN2
|aa_change=Thr236Met
|aa_change_short=T236M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17549193
|overall_frequency_n=3315
|overall_frequency_d=10758
|overall_frequency=0.308143
|n_genomes=34
|n_genomes_annotated=0
|n_haplomes=38
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.032
|nblosum100=2
|autoscore=0
|webscore=N
}}

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

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

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}