{{Rsnum
|rsid=119454949
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CACNA1H
|position=1205153
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CACNA1H
}}{{omim
|id=607904
|rsnum=119454949
|variant=0003
}}{{ClinVar
|rsid=119454949
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=1255153
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CACNA1H:8912
|GENE_NAME=CACNA1H
|GENE_ID=8912
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.1255153G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607904.0003
|CLNSIG=255
|CLNCUI=C2749872
|CLNDBN=Epilepsy, childhood absence 6
|Disease=Epilepsy
|CLNACC=RCV000002822.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2749872:611942
}}