{{Rsnum
|rsid=112084407
|Chromosome=15
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FBN1
|position=48432905
|Gene_s=FBN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=112084407
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=48725102
|CHROM=15
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000040002100100
|GENEINFO=FBN1:2200
|GENE_NAME=FBN1
|GENE_ID=2200
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.48725102C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Marfan's syndrome; AllHighlyPenetrant
|Disease=Marfan's syndrome; AllHighlyPenetrant
|Tags=RV;PM;PMC;S3D;VLD;OTHERKG;LSD
|CLNACC=RCV000029766.1; RCV000035252.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1335:C0024796:154700:558:19346006; CN169374
}}{{PMID Auto
|PMID=17253931
|Title=Rapid and efficient FBN1 mutation detection using automated sample preparation and direct sequencing as the primary strategy.
}}

{{PMID Auto
|PMID=17657824
|Title=The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193 FBN1 mutations.
}}

{{PMID Auto
|PMID=17663468
|Title=Search for correlations between FBN1 genotype and complete Ghent phenotype in 44 unrelated Norwegian patients with Marfan syndrome.
}}