{{Rsnum
|rsid=137854475
|Gene=FBN1
|Chromosome=15
|position=48487155
|Orientation=minus
|GMAF=0.0004591
|Gene_s=FBN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{omim
|id=134797
|variant=0032
|rsnum=137854475
}}{{ClinVar
|rsid=137854475
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=48779352
|CHROM=15
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=FBN1:2200
|GENE_NAME=FBN1
|GENE_ID=2200
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.48779352C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNACC=RCV000017914.22
|CLNDBN=Marfan syndrome, subdiagnostic variant of
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134797.0032
|COMMON=0
|Disease=Marfan syndrome
}}