{{Rsnum
|rsid=119103252
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PYGM
|position=64752064
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PYGM,RASGRP2
}}{{omim
|id=608455
|rsnum=119103252
|variant=0003
}}{{ClinVar
|rsid=119103252
|Reversed=1
|FwdREF=A
|FwdALT=C
|REF=T
|ALT=G
|RSPOS=64519536
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PYGM:5837
|GENE_NAME=PYGM
|GENE_ID=5837
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.64519536T>G
|CLNSRC=GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=GTR000503284; GTR000503289; 608455.0003
|CLNSIG=5
|CLNCUI=C0017924
|CLNDBN=Glycogen storage disease, type V
|Disease=Glycogen storage disease
|CLNACC=RCV000002390.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1344:C0017924:232600:368:55912009
}}