{{Rsnum
|rsid=80356680
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LAMB3
|position=209650023
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LAMB3
}}{{omim
|id=150310
|rsnum=80356680
|variant=0003
}}{{ClinVar
|rsid=80356680
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=209650023
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000605000002110100
|GENEINFO=LAMB3:3914
|GENE_NAME=LAMB3
|GENE_ID=3914
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.209650023G>A
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000228.2:c.124C>T; NBK1125; 150310.0002; 150310.0003
|CLNSIG=5
|CLNCUI=C0079683; C0268374; C0079683
|CLNDBN=Junctional epidermolysis bullosa gravis of Herlitz; Adult junctional epidermolysis bullosa
|Disease=Junctional epidermolysis bullosa gravis of Herlitz; Adult junctional epidermolysis bullosa
|CLNACC=RCV000015641.25; RCV000015642.24
|Tags=RV;PM;PMC;S3D;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1125:C0079683:226700:ORPHA79404:400140006; NBK1125:C0268374:226650:ORPHA251393:ORPHA79402:ORPHA79405:ORPHA89840:33662006
}}{{PMID Auto
|PMID=8824879
|Title=Mutational hotspots in the LAMB3 gene in the lethal (Herlitz) type of junctional epidermolysis bullosa.
}}

{{PMID Auto
|PMID=9767254
|Title=E210K mutation in the gene encoding the beta3 chain of laminin-5 (LAMB3) is predictive of a phenotype of generalized atrophic benign epidermolysis bullosa.
}}