{{Rsnum
|rsid=104894699
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNC3
|position=50323694
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNC3
}}{{omim
|id=176264
|rsnum=104894699
|variant=0001
}}{{ClinVar
|rsid=104894699
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=50826951
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=KCNC3:3748
|GENE_NAME=KCNC3
|GENE_ID=3748
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.50826951C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176264.0001
|CLNSIG=5
|CLNCUI=C1854488
|CLNDBN=Spinocerebellar ataxia 13
|Disease=Spinocerebellar ataxia 13
|CLNACC=RCV000014415.24
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1225:C1854488:605259:98768
}}