{{Rsnum
|rsid=267606993
|Chromosome=11
|position=64759898
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PYGM
|Gene_s=PYGM
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C,G
|CHROM=11
|CLNACC=RCV000002399.1
|CLNALLE=1
|CLNDBN=Glycogen storage disease, type V
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1344:C0017924:232600:368:55912009
|CLNHGVS=NC_000011.9:g.64527370T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608455.0012
|Disease=Glycogen storage disease
|FwdALT=C,G
|FwdREF=A
|GENEINFO=PYGM:5837
|GENE_ID=5837
|GENE_NAME=PYGM
|REF=T
|RSPOS=64527370
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606993
}}