Have questions? Visit https://www.reddit.com/r/SNPedia

rs589759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs589759(C;T)
Make rs589759(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position34789373
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs589759
dbSNP (old)rs589759
ClinGenrs589759
ebirs589759
HLIrs589759
Exacrs589759
Gnomadrs589759
Varsomers589759
Maprs589759
PheGenIrs589759
Biobankrs589759
1000 genomesrs589759
hgdprs589759
ensemblrs589759
gopubmedrs589759
geneviewrs589759
scholarrs589759
googlers589759
pharmgkbrs589759
gwascentralrs589759
openSNPrs589759
23andMers589759
23andMe allrs589759
SNP Nexus

SNPshotrs589759
SNPdbers589759
MSV3drs589759
GWAS Ctlgrs589759
GMAF0.365
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 23570452OA-icon.png] Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population


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


ClinVar
Risk rs589759(T;T)
Alt rs589759(T;T)
Reference Rs589759(C;C)
Significance Probable-non-pathogenic
Disease Familial restrictive cardiomyopathy Atrial septal defect Hypertrophic cardiomyopathy Left ventricular noncompaction cardiomyopathy Dilated Cardiomyopathy
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN Familial restrictive cardiomyopathy Atrial septal defect Hypertrophic cardiomyopathy Left ventricular noncompaction cardiomyopathy Dilated Cardiomyopathy, Dominant
Reversed 0
HGVS NC_000015.9:g.35081574C>T
CLNSRC
CLNACC RCV000259811.1, RCV000286985.1, RCV000317383.1, RCV000321088.1, RCV000379143.1,