{{Rsnum
|rsid=137853588
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PHKG2
|position=30756191
|Gene_s=PHKG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=172471
|variant=0002
|rsnum=137853588
}}{{ClinVar
|rsid=137853588
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=30767512
|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.30767512G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=172471.0002
|CLNSIG=5
|CLNCUI=C2751643
|CLNDBN=Glycogen storage disease IXc
|Disease=Glycogen storage disease IXc
|CLNACC=RCV000014596.23
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2751643:613027:264580
}}