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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
ebirs11556924
HLIrs11556924
Exacrs11556924
Varsomers11556924
Maprs11556924
PheGenIrs11556924
hapmaprs11556924
1000 genomesrs11556924
hgdprs11556924
ensemblrs11556924
gopubmedrs11556924
geneviewrs11556924
scholarrs11556924
googlers11556924
pharmgkbrs11556924
gwascentralrs11556924
openSNPrs11556924
23andMers11556924
23andMe allrs11556924
SNP Nexus

SNPshotrs11556924
SNPdbers11556924
MSV3drs11556924
GWAS Ctlgrs11556924
GMAF0.1919
Max Magnitude
? (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]


GET Evidence
ZC3HC1-R363H
aa_change Arg363His
aa_change_short R363H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.280535
summary



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