{{Rsnum
|rsid=387907246
|Chromosome=7
|position=66638912
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCTD7
|Gene_s=KCTD7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=7
|CLNACC=RCV000030608.1
|CLNALLE=1
|CLNDBN=EPILEPSY, PROGRESSIVE MYOCLONIC 3, WITH INTRACELLULAR INCLUSIONS
|CLNHGVS=NC_000007.13:g.66103899C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611725.0002
|Disease=EPILEPSY
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=66103899
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=387907246
|GENEINFO=KCTD7:154881
|GENE_ID=154881
|GENE_NAME=KCTD7
}}