{{Rsnum
|rsid=121913573
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LAMA2
|position=129287893
|Gene_s=LAMA2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=156225
|rsnum=121913573
|variant=0009
}}{{ClinVar
|rsid=121913573
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=129609038
|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.129609038T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=156225.0009
|CLNSIG=5
|CLNCUI=C1842898
|CLNDBN=Congenital muscular dystrophy due to partial LAMA2 deficiency
|Disease=Congenital muscular dystrophy due to partial LAMA2 deficiency
|CLNACC=RCV000015367.24
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1842898
}}