{{Rsnum
|rsid=1805031
|Gene=CACNB4
|Chromosome=2
|position=151880879
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=CACNB4
}}{{omim
|id=601949
|rsnum=1805031
|variant=0002
}}{{ClinVar
|rsid=1805031
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=152737393
|CHROM=2
|GMAF=0.0005
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050260000000000116110100
|GENEINFO=CACNB4:785
|GENE_NAME=CACNB4
|GENE_ID=785
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.152737393C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601949.0002
|CLNSIG=255
|CLNCUI=C1866039
|CLNDBN=Epilepsy, generalized idiopathic 9; Episodic ataxia, type 5
|Disease=Epilepsy; Episodic ataxia
|CLNACC=RCV000008046.1; RCV000008047.1
|Tags=RV;PM;S3D;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1866039:613855:211067
|COMMON=0
}}