{{Rsnum
|rsid=137852963
|Chromosome=20
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PANK2
|position=3912634
|Gene_s=PANK2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=606157
|variant=0006
|rsnum=137852963
}}{{ClinVar
|rsid=137852963
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=3893281
|CHROM=20
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PANK2:80025
|GENE_NAME=PANK2
|GENE_ID=80025
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.3893281G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606157.0006
|CLNSIG=5
|CLNCUI=C0018523
|CLNDBN=Pigmentary pallidal degeneration
|Disease=Pigmentary pallidal degeneration
|CLNACC=RCV000004812.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK121988:NBK1490:C0018523:234200:157850:2992000
}}