{{Rsnum
|rsid=121913571
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LAMA2
|position=129516231
|Gene_s=LAMA2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=156225
|rsnum=121913571
|variant=0005
}}{{ClinVar
|rsid=121913571
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=129837376
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=LAMA2:3908
|GENE_NAME=LAMA2
|GENE_ID=3908
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.129837376C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=156225.0005
|CLNSIG=5
|CLNCUI=C1263858
|CLNDBN=Merosin deficient congenital muscular dystrophy
|Disease=Merosin deficient congenital muscular dystrophy
|CLNACC=RCV000015361.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1291:NBK84550:NBK97333:C1263858:607855:258:111503008
}}