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rs11556924

From SNPedia

Orientationplus
Stabilizedplus
Make rs11556924(C;C)
Make rs11556924(C;T)
Make rs11556924(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position130023656
GeneZC3HC1
is asnp
is mentioned by
dbSNPrs11556924
dbSNP (classic)rs11556924
ClinGenrs11556924
ebirs11556924
HLIrs11556924
Exacrs11556924
Gnomadrs11556924
Varsomers11556924
LitVarrs11556924
Maprs11556924
PheGenIrs11556924
Biobankrs11556924
1000 genomesrs11556924
hgdprs11556924
ensemblrs11556924
geneviewrs11556924
scholarrs11556924
googlers11556924
pharmgkbrs11556924
gwascentralrs11556924
openSNPrs11556924
23andMers11556924
SNPshotrs11556924
SNPdbers11556924
MSV3drs11556924
GWAS Ctlgrs11556924
GMAF0.1919
Max Magnitude0
? (C;C) (C;T) (T;T) 28


Coronary Heart Disease

[PMID 23202125OA-icon.png] Large-scale association analysis identifies new risk loci for coronary artery disease.

[PMID 24286297OA-icon.png] The ZC3HC1 rs11556924 polymorphism is associated with increased carotid intima-media thickness in patients with rheumatoid arthritis

GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Coronary artery disease
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele T
P-val 3E-10
Odds Ratio 1.10 [1.06-1.12]
GWAS snp
PMID [PMID 21378990OA-icon.png]
Trait Coronary artery disease
Title Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Risk Allele C
P-val 9E-18
Odds Ratio 1.0900 [1.07-1.12]


[PMID 26266351OA-icon.png] Association of Zinc Finger, C3HC-Type Containing 1 (ZC3HC1) rs11556924 Genetic Variant With Hypertension in a Finnish Population, the TAMRISK Study


[PMID 27226629OA-icon.png] The Coronary Artery Disease Associated Coding Variant in Zinc finger C3HC-type containing 1 (ZC3HC1) Affects Cell Cycle Regulation.


[PMID 31679296] ADAMTS7 and ZC3HC1 Share Genetic Predisposition to Coronary Artery Disease and Large Artery Ischemic Stroke.