rs11556924

Orientation

plus

Stabilized

plus

Make rs11556924(C;C)

Make rs11556924(C;T)

Make rs11556924(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

130023656

Gene

ZC3HC1

is a	snp
is	mentioned by
dbSNP	rs11556924
dbSNP (classic)	rs11556924
ClinGen	rs11556924
ebi	rs11556924
HLI	rs11556924
Exac	rs11556924
Gnomad	rs11556924
Varsome	rs11556924
LitVar	rs11556924
Map	rs11556924
PheGenI	rs11556924
Biobank	rs11556924
1000 genomes	rs11556924
hgdp	rs11556924
ensembl	rs11556924
geneview	rs11556924
scholar	rs11556924
google	rs11556924
pharmgkb	rs11556924
gwascentral	rs11556924
openSNP	rs11556924
23andMe	rs11556924
SNPshot	rs11556924
SNPdbe	rs11556924
MSV3d	rs11556924
GWAS Ctlg	rs11556924

GMAF

0.1919

Max Magnitude

0

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

Coronary Heart Disease

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

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

GWAS snp
PMID	[PMID 24262325]
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 21378990]
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 26266351] 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.

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