{{Rsnum
|rsid=80338767
|Chromosome=14
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FBLN5
|position=91877501
|Gene_s=FBLN5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338767
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=92343845
|CHROM=14
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=FBLN5:10516
|GENE_NAME=FBLN5
|GENE_ID=10516
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.92343845C>A
|CLNORIGIN=0
|CLNSIG=5
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000020639.2
|CLNDBN=Autosomal recessive cutis laxa type IA
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK5201:NBK54467:CN033664:219100:90349:59451000
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK5201; 604580.0011
|Disease=Autosomal recessive cutis laxa type IA
}}