{{Rsnum
|rsid=121908987
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PRKAG2
|position=151576412
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRKAG2
}}{{omim
|id=602743
|rsnum=121908987
|variant=0001
}}{{ClinVar
|rsid=121908987
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=151273498
|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
|CLNHGVS=NC_000007.13:g.151273498C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602743.0001
|CLNSIG=5
|CLNCUI=C0043202; C1833236
|CLNDBN=Wolff-Parkinson-White pattern; Familial hypertrophic cardiomyopathy 6; Primary familial hypertrophic cardiomyopathy
|Disease=Wolff-Parkinson-White pattern; Familial hypertrophic cardiomyopathy 6; Primary familial hypertrophic cardiomyopathy
|CLNACC=RCV000007248.1; RCV000007249.1; RCV000038960.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT; GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=C0043202:194200:74390002; NBK1768:C1833236:600858; NBK1768:C0949658:83978005
}}