{{Rsnum
|rsid=28357092
|Gene=FCN3
|Chromosome=1
|position=27373182
|Orientation=minus
|GMAF=0.01515
|Gene_s=FCN3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
}}{{omim
|id=604973
|rsnum=28357092
|variant=0001
}}

{{PMID|19535802}} Immunodeficiency associated with FCN3 mutation and ficolin-3 deficiency.

{{GET Evidence
|gene=FCN3
|aa_change=Leu117Shift
|aa_change_short=L117Shift
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs28357092
|overall_frequency_n=3
|overall_frequency_d=128
|overall_frequency=0.0234375
|n_genomes=3
|n_genomes_annotated=0
|n_haplomes=3
|n_articles=0
|n_articles_annotated=0
|nblosum100=4
|autoscore=2
|webscore=N
}}

{{PMID Auto
|PMID=23142462
|Title=A novel assay to quantitate MASP-2/ficolin-3 complexes in serum
}}

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

{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000005603.2
|CLNALLE=1
|CLNDBN=Immunodeficiency due to ficolin 3 deficiency
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151226:613860
|CLNHGVS=NC_000001.11:g.27373180delG
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_003665.2:c.349delC; 604973.0001
|Disease=Immunodeficiency due to ficolin 3 deficiency
|FwdREF=C
|GENEINFO=FCN3:8547
|GENE_ID=8547
|GENE_NAME=FCN3
|REF=AG
|RSPOS=27373179
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;NSF;NSM;REF;ASP;VLD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;OM;NOC
|VC=DIV
|VP=0x050268001a0514011e010210
|WGT=1
|dbSNPBuildID=125
|rsid=28357092
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}