{{Rsnum
|rsid=121918021
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=PHKB
|position=47596425
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PHKB
}}{{omim
|id=172490
|rsnum=121918021
|variant=0003
}}{{ClinVar
|rsid=121918021
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=47630336
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PHKB:5257
|GENE_NAME=PHKB
|GENE_ID=5257
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.47630336T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=172490.0003
|CLNSIG=5
|CLNCUI=C1849812
|CLNDBN=Glycogen storage disease IXb
|Disease=Glycogen storage disease IXb
|CLNACC=RCV000014590.24
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK55061:C1849812:261750:79240
}}