{{Rsnum
|rsid=144081869
|Chromosome=11
|position=64750497
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PYGM
|Gene_s=PYGM
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000002396.1
|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.64517969C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608455.0008
|Disease=Glycogen storage disease
|FwdALT=T
|FwdREF=C
|GENEINFO=PYGM:5837
|GENE_ID=5837
|GENE_NAME=PYGM
|REF=C
|RSPOS=64517969
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=144081869
}}