{{Rsnum
|rsid=116987552
|Gene=PYGM
|Chromosome=11
|position=64759751
|Orientation=plus
|GMAF=0.001377
|Gene_s=PYGM,RASGRP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{omim
|id=608455
|rsnum=116987552
|variant=0001
}}{{ClinVar
|rsid=116987552
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=64527223
|CHROM=11
|GMAF=0.0014
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=PYGM:5837
|GENE_NAME=PYGM
|GENE_ID=5837
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.64527223G>A
|CLNSRC=Emory University; GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=1770; GTR000503284; GTR000503289; 608455.0001
|CLNSIG=5
|CLNCUI=C0017924
|CLNDBN=Glycogen storage disease, type V; not provided
|Disease=Glycogen storage disease; not provided
|CLNACC=RCV000002388.1; RCV000081306.1
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1344:C0017924:232600:368:55912009
|COMMON=0
}}