{{Rsnum
|rsid=104894205
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CSRP3
|position=19188286
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CSRP3
}}{{omim
|id=600824
|rsnum=104894205
|variant=0003
}}{{ClinVar
|rsid=104894205
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=19209833
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CSRP3:8048
|GENE_NAME=CSRP3
|GENE_ID=8048
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.19209833A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600824.0003
|CLNSIG=5
|CLNCUI=CN029460
|CLNDBN=Familial hypertrophic cardiomyopathy 12; AllHighlyPenetrant
|Disease=Familial hypertrophic cardiomyopathy 12; AllHighlyPenetrant
|CLNACC=RCV000009323.2; RCV000037770.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM; MedGen
|CLNDSDBID=CN029460:612124; CN169374
}}