{{Rsnum
|rsid=121434549
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CASQ2
|position=115705212
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CASQ2
}}{{omim
|id=114251
|rsnum=121434549
|variant=0001
}}{{ClinVar
|rsid=121434549
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=115705212
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=CASQ2:845
|GENE_NAME=CASQ2
|GENE_ID=845
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.115705212C>G
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001232.3:c.919G>C; NBK1289; 114251.0001
|CLNSIG=5
|CLNCUI=C2677794
|CLNDBN=Ventricular tachycardia, catecholaminergic polymorphic, 2
|Disease=Ventricular tachycardia
|CLNACC=RCV000019176.27
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1289:C2677794:611938:ORPHA3286
}}