{{Rsnum
|rsid=113871094
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FBN1
|position=48465820
|Gene_s=FBN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=113871094
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=48758017
|CHROM=15
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|GENEINFO=FBN1:2200
|GENE_NAME=FBN1
|GENE_ID=2200
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.48758017G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Marfan's syndrome
|Disease=Marfan's syndrome
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029744.2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1335:C0024796:154700:558:19346006
}}{{PMID Auto
|PMID=15241
|Title=Population policy 1977: a reexamination of the issues.
}}

{{PMID Auto
|PMID=11700157
|Title=Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome.
}}

{{PMID Auto
|PMID=11933199
|Title=Evaluation and application of denaturing HPLC for mutation detection in Marfan syndrome: Identification of 20 novel mutations and two novel polymorphisms in the FBN1 gene.
}}

{{PMID Auto
|PMID=16756980
|Title=Preimplantation genetic diagnosis for Marfan syndrome.
}}

{{PMID Auto
|PMID=17718856
|Title=Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndrome.
}}

{{PMID Auto
|PMID=19618372
|Title=Quantitative sequence analysis of FBN1 premature termination codons provides evidence for incomplete NMD in leukocytes.
}}