{{Rsnum
|rsid=387906830
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VRK1
|position=96852853
|Gene_s=VRK1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Chromosome=14
}}{{ClinVar
|ALT=T
|CHROM=14
|CLNACC=RCV000023167.2
|CLNALLE=1
|CLNDBN=Pontocerebellar hypoplasia type 1
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1843504:607596:2254
|CLNHGVS=NC_000014.8:g.97319190C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602168.0002
|Disease=Pontocerebellar hypoplasia type 1
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=97319190
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906830
|GENEINFO=VRK1:7443
|GENE_ID=7443
|GENE_NAME=VRK1
}}