{{Rsnum
|rsid=397514579
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRRT2
|position=29813802
|Gene_s=LOC100289283,PRRT2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=16
|CLNACC=RCV000032974.1; RCV000032975.1
|CLNALLE=1
|CLNDBN=Dystonia 10; Seizures, benign familial infantile, 2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1460:C1868682:128200:98809; C1853995:605751:306
|CLNHGVS=NC_000016.9:g.29825123C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614386.0015
|Disease=Dystonia 10; Seizures
|FwdALT=T
|FwdREF=C
|GENEINFO=LOC100289283:100289283; PRRT2:112476
|GENE_ID=100289283; 112476
|GENE_NAME=LOC100289283; PRRT2
|REF=C
|RSPOS=29825123
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514579
}}