{{Rsnum
|rsid=137854467
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FBN1
|position=48600217
|Gene_s=FBN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134797
|variant=0018
|rsnum=137854467
}}{{ClinVar
|rsid=137854467
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=48892414
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=FBN1:2200
|GENE_NAME=FBN1
|GENE_ID=2200
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.48892414G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNACC=RCV000017902.26; RCV000029732.1
|CLNDBN=Marfan syndrome, atypical; Marfan's syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1335:C0024796:154700:558:19346006
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134797.0018
|Disease=Marfan syndrome; Marfan's syndrome
}}{{PMID Auto
|PMID=17657
|Title=Base-catalyzed reactions of 1,3-disubstituted uracils.
}}

{{PMID Auto
|PMID=12446365
|Title=Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitus.
|OA=1
}}

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

{{PMID Auto
|PMID=18087243
|Title=Is ectopia lentis in some cases a mild phenotypic expression of Marfan syndrome? Need for a long-term follow-up.
}}

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

{{PMID Auto
|PMID=19328768
|Title=Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis.
}}