{{Rsnum
|rsid=25403
|Chromosome=15
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FBN1
|position=48613073
|Gene_s=FBN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 98.1 | 1.9 | 0.0
| MEX | 96.6 | 3.4 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 99.0 | 1.0 | 0.0
| HapMapRevision=28
}}{{ClinVar
|ALT=A
|CHROM=15
|CLNACC=RCV000035129.1
|CLNALLE=1
|CLNDBN=Marfan's syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1335:C0024796:154700:558:19346006
|CLNHGVS=NC_000015.9:g.48905270G>A
|CLNSIG=5
|Disease=Marfan's syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=FBN1:2200
|GENE_ID=2200
|GENE_NAME=FBN1
|REF=G
|RSPOS=48905270
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;VLD;HD;GNO;OTHERKG;PH3;LSD;OM
|VC=SNV
|VP=0x050060000000040503110100
|WGT=0
|dbSNPBuildID=69
|rsid=25403
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}