{{Rsnum
|rsid = 28938173
|Gene = PRKAG2
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=7
|position=151568750
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRKAG2
}}[[Familial hypertrophic cardiomyopathy]]

see also OMIM [http://omim.org/entry/602743#0004 602743.0004]

{{omim
|desc=CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, WITH WOLFF-PARKINSON-WHITE SYNDROME
|id=602743
|rsnum=28938173
|variant=0004
}}

{{ClinVar
|rsid=28938173
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=151265836
|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.151265836G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602743.0004
|CLNSIG=5
|CLNCUI=C1833236
|CLNDBN=Familial hypertrophic cardiomyopathy 6; Primary familial hypertrophic cardiomyopathy
|Disease=Familial hypertrophic cardiomyopathy 6; Primary familial hypertrophic cardiomyopathy
|CLNACC=RCV000007252.1; RCV000038910.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C1833236:600858; NBK1768:C0949658:83978005
}}

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