{{Rsnum
|rsid=121918113
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ATP2A1
|position=28887236
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP2A1
}}{{omim
|id=108730
|rsnum=121918113
|variant=0001
}}{{ClinVar
|rsid=121918113
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=28898557
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ATP2A1:487
|GENE_NAME=ATP2A1
|GENE_ID=487
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.28898557C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=108730.0001
|CLNSIG=5
|CLNCUI=C1832918
|CLNDBN=Brody myopathy
|Disease=Brody myopathy
|CLNACC=RCV000019380.22
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1832918:601003:53347
}}