rs533021

Orientation

plus

Stabilized

plus

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

Make rs533021(C;C)

Make rs533021(C;T)

Reference

GRCh38 38.1/141

Chromosome

15

Position

34788730

Gene	ACTC1, LOC101928174

is a	snp
is	mentioned by
dbSNP	rs533021
dbSNP (classic)	rs533021
ClinGen	rs533021
ebi	rs533021
HLI	rs533021
Exac	rs533021
Gnomad	rs533021
Varsome	rs533021
LitVar	rs533021
Map	rs533021
PheGenI	rs533021
Biobank	rs533021
1000 genomes	rs533021
hgdp	rs533021
ensembl	rs533021
geneview	rs533021
scholar	rs533021
google	rs533021
pharmgkb	rs533021
gwascentral	rs533021
openSNP	rs533021
23andMe	rs533021
SNPshot	rs533021
SNPdbe	rs533021
MSV3d	rs533021
GWAS Ctlg	rs533021

GMAF

0.4766

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 23570452] Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population

[PMID 20592870] Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genes.

ClinVar
Risk	rs533021(C;C)
Alt	rs533021(C;C)
Reference	Rs533021(T;T)
Significance	Probable-non-pathogenic
Disease	Left ventricular noncompaction cardiomyopathy Dilated Cardiomyopathy Atrial septal defect Hypertrophic cardiomyopathy Familial restrictive cardiomyopathy
Variation	info
Gene	ACTC1 LOC101928174 RP11-814P5.1
CLNDBN	Left ventricular noncompaction cardiomyopathy Dilated Cardiomyopathy, Dominant Atrial septal defect Hypertrophic cardiomyopathy Familial restrictive cardiomyopathy
Reversed	0
HGVS	NC_000015.9:g.35080931T>C
CLNSRC
CLNACC	RCV000284649.1, RCV000309165.1, RCV000339715.1, RCV000394697.1, RCV000406244.1,