{{Rsnum
|rsid=121912938
|Chromosome=21
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COL6A1
|position=45989129
|Gene_s=COL6A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=120220
|rsnum=121912938
|variant=0012
}}{{ClinVar
|rsid=121912938
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=47409043
|CHROM=21
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=COL6A1:1291
|GENE_NAME=COL6A1
|GENE_ID=1291
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.47409043G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000018720.26; RCV000079828.1
|CLNDBN=Ullrich congenital muscular dystrophy, autosomal dominant; not provided
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNSRCID=7503; 120220.0012
|Disease=Ullrich congenital muscular dystrophy; not provided
}}