{{Rsnum
|rsid=121434548
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CAPN3
|position=42401755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAPN3
}}{{omim
|id=114240
|rsnum=121434548
|variant=0010
}}{{ClinVar
|rsid=121434548
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=42693953
|CHROM=15
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CAPN3:825
|GENE_NAME=CAPN3
|GENE_ID=825
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.42693953G>A
|CLNSRC=GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=GTR000330880; 114240.0010
|CLNSIG=5
|CLNCUI=C1869123
|CLNDBN=Limb-girdle muscular dystrophy, type 2A
|Disease=Limb-girdle muscular dystrophy
|CLNACC=RCV000019189.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1313:NBK1408:C1869123:253600:267
}}