{{Rsnum
|rsid=104894358
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNA1
|position=4912627
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNA1
}}{{omim
|id=176260
|rsnum=104894358
|variant=0012
}}{{ClinVar
|rsid=104894358
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=5021793
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=KCNA1:3736
|GENE_NAME=KCNA1
|GENE_ID=3736
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.5021793C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK25442; 176260.0012
|CLNSIG=5
|CLNCUI=C1719788; C1719788
|CLNDBN=Episodic ataxia type 1
|Disease=Episodic ataxia type 1
|CLNACC=RCV000014435.24
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK25442:C1719788:160120:421182009
}}