{{Rsnum
|rsid=121912483
|Chromosome=1
|position=209634515
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LAMB3
|Gene_s=LAMB3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=150310
|rsnum=121912483
|variant=0007
}}{{ClinVar
|rsid=121912483
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=209634515
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=LAMB3:3914
|GENE_NAME=LAMB3
|GENE_ID=3914
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.209634515G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000228.2:c.496C>T; 150310.0007
|CLNSIG=5
|CLNCUI=C0079683
|CLNDBN=Junctional epidermolysis bullosa gravis of Herlitz
|Disease=Junctional epidermolysis bullosa gravis of Herlitz
|CLNACC=RCV000015645.24
|Tags=RV;PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1125:C0079683:226700:ORPHA79404:400140006
}}