rs267606977

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	6.2	Familial Hypertrophic Cardiomyopathy

Make rs267606977(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

151560613

Gene

PRKAG2

is a	snp
is	mentioned by
dbSNP	rs267606977
dbSNP (classic)	rs267606977
ClinGen	rs267606977
ebi	rs267606977
HLI	rs267606977
Exac	rs267606977
Gnomad	rs267606977
Varsome	rs267606977
LitVar	rs267606977
Map	rs267606977
PheGenI	rs267606977
Biobank	rs267606977
1000 genomes	rs267606977
hgdp	rs267606977
ensembl	rs267606977
geneview	rs267606977
scholar	rs267606977
google	rs267606977
pharmgkb	rs267606977
gwascentral	rs267606977
openSNP	rs267606977
23andMe	rs267606977
SNPshot	rs267606977
SNPdbe	rs267606977
MSV3d	rs267606977
GWAS Ctlg	rs267606977

Max Magnitude

6.2

ClinVar
Risk	rs267606977(G;G)
Alt	rs267606977(G;G)
Reference	Rs267606977(A;A)
Significance	Pathogenic
Disease	Familial hypertrophic cardiomyopathy 6 not provided
Variation	info
Gene	PRKAG2
CLNDBN	Familial hypertrophic cardiomyopathy 6 not provided
Reversed	1
HGVS	NC_000007.13:g.151257699T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007257.4, RCV000159018.1,