{{Rsnum
|rsid=137854480
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FBN1
|position=48537629
|Gene_s=FBN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134797
|variant=0042
|rsnum=137854480
}}{{ClinVar
|rsid=137854480
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=48829826
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=FBN1:2200
|GENE_NAME=FBN1
|GENE_ID=2200
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.48829826G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=134797.0042
|CLNSIG=5
|CLNCUI=C0024796; C1851286
|CLNDBN=Marfan's syndrome; Ectopia lentis, isolated, autosomal dominant
|Disease=Marfan's syndrome; Ectopia lentis
|CLNACC=RCV000017924.27; RCV000017925.26
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1335:C0024796:154700:558:19346006; C1851286:129600:1885
}}{{PMID|12203}} 13C NMR studies of ferrous citrates in acidic and alkaline solutions. Implications concerning the active site of aconitase.

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

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

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

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

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