rs193922697

Orientation

minus

Stabilized

minus

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

Make rs193922697(A;A)

Make rs193922697(A;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

151576438

Gene

PRKAG2

is a	snp
is	mentioned by
dbSNP	rs193922697
dbSNP (classic)	rs193922697
ClinGen	rs193922697
ebi	rs193922697
HLI	rs193922697
Exac	rs193922697
Gnomad	rs193922697
Varsome	rs193922697
LitVar	rs193922697
Map	rs193922697
PheGenI	rs193922697
Biobank	rs193922697
1000 genomes	rs193922697
hgdp	rs193922697
ensembl	rs193922697
geneview	rs193922697
scholar	rs193922697
google	rs193922697
pharmgkb	rs193922697
gwascentral	rs193922697
openSNP	rs193922697
23andMe	rs193922697
SNPshot	rs193922697
SNPdbe	rs193922697
MSV3d	rs193922697
GWAS Ctlg	rs193922697

Max Magnitude

0

ClinVar
Risk	rs193922697(A;A) rs193922697(T;T)
Alt	rs193922697(A;A) rs193922697(T;T)
Reference	Rs193922697(C;C)
Significance	Probable-Pathogenic
Disease	Cardiomyopathy
Variation	info
Gene	PRKAG2
CLNDBN	Cardiomyopathy
Reversed	1
HGVS	NC_000007.13:g.151273524G>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030377.1,