{{Rsnum
|rsid=118203899
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=LAMC2
|position=183225719
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LAMC2
}}{{omim
|id=150292
|rsnum=118203899
|variant=0003
}}{{ClinVar
|rsid=118203899
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=183225719
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000605000002110100
|GENEINFO=LAMC2:3918
|GENE_NAME=LAMC2
|GENE_ID=3918
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.183225719C>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005562.2:c.1065C>G; 150292.0003
|CLNSIG=5
|CLNCUI=C0079683
|CLNDBN=Junctional epidermolysis bullosa gravis of Herlitz
|Disease=Junctional epidermolysis bullosa gravis of Herlitz
|CLNACC=RCV000015657.24
|Tags=PM;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1125:C0079683:226700:ORPHA79404:400140006
}}