{{Rsnum
|rsid=121913577
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=LAMA2
|position=129297729
|Gene_s=LAMA2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=156225
|rsnum=121913577
|variant=0013
}}{{ClinVar
|rsid=121913577
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=129618874
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=LAMA2:3908
|GENE_NAME=LAMA2
|GENE_ID=3908
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.129618874C>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK97333; 156225.0013
|CLNSIG=5
|CLNCUI=C1263858
|CLNDBN=Merosin deficient congenital muscular dystrophy
|Disease=Merosin deficient congenital muscular dystrophy
|CLNACC=RCV000015371.24
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1291:NBK84550:NBK97333:C1263858:607855:258:111503008
}}