{{Rsnum
|rsid=121434546
|Chromosome=15
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CAPN3
|position=42360062
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAPN3
}}{{omim
|id=114240
|rsnum=121434546
|variant=0004
}}{{ClinVar
|rsid=121434546
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=42652260
|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.42652260C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=114240.0004
|CLNSIG=5
|CLNCUI=C1869123
|CLNDBN=Limb-girdle muscular dystrophy, type 2A
|Disease=Limb-girdle muscular dystrophy
|CLNACC=RCV000019182.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1313:NBK1408:C1869123:253600:267
}}