rs267606979

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;T)	6.2	Familial Hypertrophic Cardiomyopathy
(T;T)	0	common in clinvar

Make rs267606979(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

151560560

Gene

PRKAG2

is a	snp
is	mentioned by
dbSNP	rs267606979
dbSNP (classic)	rs267606979
ClinGen	rs267606979
ebi	rs267606979
HLI	rs267606979
Exac	rs267606979
Gnomad	rs267606979
Varsome	rs267606979
LitVar	rs267606979
Map	rs267606979
PheGenI	rs267606979
Biobank	rs267606979
1000 genomes	rs267606979
hgdp	rs267606979
ensembl	rs267606979
geneview	rs267606979
scholar	rs267606979
google	rs267606979
pharmgkb	rs267606979
gwascentral	rs267606979
openSNP	rs267606979
23andMe	rs267606979
SNPshot	rs267606979
SNPdbe	rs267606979
MSV3d	rs267606979
GWAS Ctlg	rs267606979

Max Magnitude

6.2

ClinVar
Risk	rs267606979(C;C)
Alt	rs267606979(C;C)
Reference	Rs267606979(T;T)
Significance	Pathogenic
Disease	Familial hypertrophic cardiomyopathy 6
Variation	info
Gene	PRKAG2
CLNDBN	Familial hypertrophic cardiomyopathy 6
Reversed	1
HGVS	NC_000007.13:g.151257646A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007259.2,