{{Rsnum
|rsid=387907125
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PRRT2
|position=29814403
|Gene_s=C16orf53,PRRT2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=16
|CLNACC=RCV000024170.1
|CLNALLE=1
|CLNDBN=Infantile convulsions and paroxysmal choreoathetosis, familial
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1865926:602066:31709
|CLNHGVS=NC_000016.9:g.29825724G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614386.0005
|Disease=Infantile convulsions and paroxysmal choreoathetosis
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=29825724
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907125
|GENEINFO=PAGR1:79447; PRRT2:112476
|GENE_ID=79447; 112476
|GENE_NAME=PAGR1; PRRT2
}}