{{Rsnum
|rsid = 28939088
|Gene = PANK2
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|Chromosome=20
|position=3912532
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PANK2
}}{{omim
|desc=HARP SYNDROME
|id=606157
|rsnum=28939088
|variant=0012
}}

{{ClinVar
|rsid=28939088
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=3893179
|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.3893179T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606157.0012
|CLNSIG=5
|CLNCUI=C1846582
|CLNDBN=Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration
|Disease=Hypoprebetalipoproteinemia
|CLNACC=RCV000004819.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1490:C1846582:607236
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}