{{Rsnum
|rsid=121913574
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LAMA2
|position=129190317
|Gene_s=LAMA2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=156225
|rsnum=121913574
|variant=0010
}}{{ClinVar
|rsid=121913574
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=129511462
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=LAMA2:3908
|GENE_NAME=LAMA2
|GENE_ID=3908
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.129511462G>A
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=9746; 156225.0010
|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=RCV000015368.24; RCV000078747.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1842898
}}