{{Rsnum
|rsid=137853591
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PHKG2
|position=30753434
|Gene_s=PHKG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=172471
|variant=0006
|rsnum=137853591
}}{{ClinVar
|rsid=137853591
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=30764755
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PHKG2:5261
|GENE_NAME=PHKG2
|GENE_ID=5261
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.30764755C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=172471.0006
|CLNSIG=5
|CLNCUI=C2751643
|CLNDBN=Glycogen storage disease IXc
|Disease=Glycogen storage disease IXc
|CLNACC=RCV000014600.23
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2751643:613027:264580
}}