{{Rsnum
|rsid=193922228
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FBN1
|position=48430736
|Gene_s=FBN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922228
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=48722933
|CHROM=15
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.48722933A>G
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Marfan's syndrome
|Disease=Marfan's syndrome
|Tags=RV;PM;PMC;OTHERKG;LSD
|CLNACC=RCV000029769.2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1335:C0024796:154700:558:19346006
|GENEINFO=FBN1:2200
|GENE_ID=2200
|GENE_NAME=FBN1
}}{{PMID Auto
|PMID=16342
|Title=Cardiac pacemaking: an obligatory role of catecholamines?
}}

{{PMID Auto
|PMID=10464652
|Title=Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders.
}}

{{PMID Auto
|PMID=12203992
|Title=TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies.
}}

{{PMID Auto
|PMID=12938084
|Title=Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database.
}}

{{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=19159394
|Title=Prevalence of dural ectasia in 63 gene-mutation-positive patients with features of Marfan syndrome type 1 and Loeys-Dietz syndrome and report of 22 novel FBN1 mutations.
}}