{{Rsnum
|rsid=397515476
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=KCND3
|position=111981673
|Gene_s=KCND3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=1
|CLNACC=RCV000056299.1
|CLNALLE=1
|CLNDBN=Spinocerebellar ataxia 19
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1138:C1846367:607346:ORPHA98772
|CLNHGVS=NC_000001.11:g.111981673T>G
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_004980.4:c.1054A>C; 605411.0002
|Disease=Spinocerebellar ataxia 19
|FwdALT=C
|FwdREF=A
|GENEINFO=KCND3:3752
|GENE_ID=3752
|GENE_NAME=KCND3
|REF=T
|RSPOS=111981673
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=136
|rsid=397515476
|CLNORIGIN=1
}}