{{Rsnum
|rsid=137852289
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PHKA2
|position=18940017
|Gene_s=PHKA2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300798
|variant=0007
|rsnum=137852289
}}{{ClinVar
|rsid=137852289
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=18958135
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PHKA2:5256
|GENE_NAME=PHKA2
|GENE_ID=5256
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.18958135T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300798.0007
|CLNSIG=5
|CLNCUI=C1418533
|CLNDBN=Glycogen storage disease type IXa1
|Disease=Glycogen storage disease type IXa1
|CLNACC=RCV000011280.3
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK55061:C0017927:306000:264580
}}