{{Rsnum
|rsid=111401431
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FBN1
|position=48468097
|Gene_s=FBN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111401431
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=48760294
|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.48760294G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Marfan's syndrome
|Disease=Marfan's syndrome
|Tags=RV;PM;PMC;S3D;VLD;OTHERKG;LSD
|CLNACC=RCV000029740.2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1335:C0024796:154700:558:19346006
}}{{PMID Auto
|PMID=19941
|Title=Cerebral hemodynamic and metabolic alterations in hypovolemic shock.
}}

{{PMID Auto
|PMID=15054843
|Title=Ectopia lentis phenotypes and the FBN1 gene.
}}

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

{{PMID Auto
|PMID=18615205
|Title=Late-onset bilateral lens dislocation and glaucoma associated with a novel mutation in FBN1.
|OA=1
}}

{{PMID Auto
|PMID=19863550
|Title=Clinical and genetic analysis of Korean patients with Marfan syndrome: possible ethnic differences in clinical manifestation.
}}