{{Rsnum
|rsid=34667348
|Gene=PHKB
|Chromosome=16
|position=47650919
|Orientation=plus
|GMAF=0.002296
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=PHKB
}}{{omim
|id=172490
|rsnum=34667348
|variant=0002
}}

{{ClinVar
|rsid=34667348
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=47684830
|CHROM=16
|GMAF=0.0023
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050160000000040116110100
|GENEINFO=PHKB:5257
|GENE_NAME=PHKB
|GENE_ID=5257
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000016.9:g.47684830C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=172490.0002
|CLNSIG=5
|CLNCUI=C1849812
|CLNDBN=Glycogen storage disease IXb
|Disease=Glycogen storage disease IXb
|CLNACC=RCV000014588.24
|Tags=PM;SLO;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9977; 0.002296; .
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK55061:C1849812:261750:79240
|COMMON=0
}}

{{on chip | FTDNA2}}
{{on chip | FTDNA}}