{{Rsnum
|rsid=121913576
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LAMA2
|position=129464444
|Gene_s=LAMA2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=156225
|rsnum=121913576
|variant=0012
}}{{ClinVar
|rsid=121913576
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=129785589
|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.129785589C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=8381; 156225.0012
|CLNSIG=5
|CLNCUI=C1842898
|CLNDBN=Congenital muscular dystrophy due to partial LAMA2 deficiency; not provided
|Disease=Congenital muscular dystrophy due to partial LAMA2 deficiency; not provided
|CLNACC=RCV000015370.24; RCV000078794.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1842898
}}