{{Rsnum
|rsid=1805032
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CACNB4
|position=151839238
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CACNB4
}}{{omim
|id=601949
|rsnum=1805032
|variant=0001
}}{{ClinVar
|rsid=1805032
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=152695752
|CHROM=2
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050060000000000102110100
|GENEINFO=CACNB4:785
|GENE_NAME=CACNB4
|GENE_ID=785
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.152695752G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601949.0001
|CLNSIG=255
|CLNCUI=CN043198
|CLNDBN=Epilepsy, juvenile myoclonic 6
|Disease=Epilepsy
|CLNACC=RCV000008045.1
|Tags=RV;PM;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN043198
}}