{{Rsnum
|rsid=267607199
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCTD7
|position=66633425
|Gene_s=KCTD7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=7
|CLNACC=RCV000000886.1
|CLNALLE=1
|CLNDBN=Epilepsy, progressive myoclonic 3
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2673257:611726:263516
|CLNHGVS=NC_000007.13:g.66098412C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611725.0001
|Disease=Epilepsy
|FwdALT=T
|FwdREF=C
|GENEINFO=KCTD7:154881
|GENE_ID=154881
|GENE_NAME=KCTD7
|REF=C
|RSPOS=66098412
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607199
}}