rs267606976

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs267606976(C;C)

Make rs267606976(C;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

151564203

Gene

PRKAG2

is a	snp
is	mentioned by
dbSNP	rs267606976
dbSNP (classic)	rs267606976
ClinGen	rs267606976
ebi	rs267606976
HLI	rs267606976
Exac	rs267606976
Gnomad	rs267606976
Varsome	rs267606976
LitVar	rs267606976
Map	rs267606976
PheGenI	rs267606976
Biobank	rs267606976
1000 genomes	rs267606976
hgdp	rs267606976
ensembl	rs267606976
geneview	rs267606976
scholar	rs267606976
google	rs267606976
pharmgkb	rs267606976
gwascentral	rs267606976
openSNP	rs267606976
23andMe	rs267606976
SNPshot	rs267606976
SNPdbe	rs267606976
MSV3d	rs267606976
GWAS Ctlg	rs267606976

Max Magnitude

0

ClinVar
Risk	rs267606976(C;C)
Alt	rs267606976(C;C)
Reference	Rs267606976(T;T)
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.151261289A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007256.6, RCV000159015.2,