{{Rsnum
|rsid=10250779
|Gene=PGAM2
|Chromosome=7
|position=44065297
|Orientation=plus
|ReferenceAllele=G
|GMAF=0.001837
|Gene_s=BOLA3-AS1,PGAM2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}Several African-American [[rs10250779]](T;T) homozygotes (as oriented in dbSNP) have been reported to experience intense muscle pain and cramps upon exercising. It is not known what percentage of such homozgyotes respond to exercise in this manner.{{PMID|8447317|OA=1
}}

{{omim
| id = 261670
| variant = 0001
| desc    = MYOPATHY DUE TO DEFICIENCY OF MUSCLE PHOSPHOGLYCERATE MUTASE
| rsnum   = 10250779
}}

{{omim
|id=612931
|rsnum=10250779
|variant=0001
}}

{{ClinVar
|rsid=10250779
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=44104896
|CHROM=7
|GMAF=0.0018
|dbSNPBuildID=119
|SSR=0
|SAO=1
|VP=0x050268000000040517110100
|GENEINFO=PGAM2:5224
|GENE_NAME=PGAM2
|GENE_ID=5224
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.44104896C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612931.0001
|CLNSIG=5
|CLNCUI=C0268149
|CLNDBN=Glycogen storage disease type X
|Disease=Glycogen storage disease type X
|CLNACC=RCV000000446.1
|Tags=RV;PM;PMC;S3D;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9982; 0.001837
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268149:261670:97234:37666005
|COMMON=1
}}

{{PMID|18852891|OA=1
}} Distribution and effects of nonsense polymorphisms in human genes.

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}