{{Rsnum
|rsid=121908991
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PRKAG2
|position=151560610
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRKAG2
}}{{omim
|id=602743
|rsnum=121908991
|variant=0007
}}{{ClinVar
|rsid=121908991
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=151257696
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PRKAG2:51422
|GENE_NAME=PRKAG2
|GENE_ID=51422
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000007.13:g.151257696C>A; NC_000007.13:g.151257696C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602743.0007
|CLNSIG=5
|CLNCUI=C1849813
|CLNDBN=AllHighlyPenetrant; Glycogen storage disease of heart, lethal congenital; Primary familial hypertrophic cardiomyopathy
|Disease=AllHighlyPenetrant; Glycogen storage disease of heart; Primary familial hypertrophic cardiomyopathy
|CLNACC=RCV000038921.1; RCV000007255.1; RCV000038920.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen; MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=CN169374; C1849813:261740; NBK1768:C0949658:83978005
}}