{{Rsnum
|rsid=137853063
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VRK1
|position=96876033
|Gene_s=VRK1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=602168
|variant=0001
|rsnum=137853063
}}{{ClinVar
|rsid=137853063
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=97342370
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=VRK1:7443
|GENE_NAME=VRK1
|GENE_ID=7443
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.97342370C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602168.0001
|CLNSIG=5
|CLNCUI=C1843504
|CLNDBN=Pontocerebellar hypoplasia type 1
|Disease=Pontocerebellar hypoplasia type 1
|CLNACC=RCV000007926.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1843504:607596:2254
}}