Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE Regarding ZC3HC1 rs11556924, our study further supports the observed association of rs11556924 with LA IS coming from previous GWASs. 31679296 2019
dbSNP: rs1464890
rs1464890
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE In the genetic model analysis, we identified that the SNP of rs1464890 in ZC3HC1 was associated with a 0.68-fold decreased risk of hypertension in the codominant model and 0.65-fold decreased risk in the dominant model. 31507094 2019
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE These findings extend the genetic association between rs11556924 and coronary artery disease risk by characterizing its effects on the encoded protein, NIPA. 28115489 2017
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE A subpopulation that had available follow-up data from ages of 40, 45, and 50 years was also analyzed.ZC3HC1 rs11556924 (C > T) genotype CC was associated with hypertension compared with the T-allele carriers (P = 0.013). 26266351 2015
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0085580
Disease:
Essential Hypertension
0.010 GeneticVariation BEFREE Its major TT-genotype was associated with higher total cholesterol (P = 0.044) and LDL (P = 0.029) compared with the C-allele.We report for the first time that ZC3HC1 rs11556924 was associated with essential hypertension in 50-year-old patients. 26266351 2015
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.010 GeneticVariation BEFREE Our results indicate that ZC3HC1 rs11556924 polymorphism is associated with subclinical atherosclerosis in RA. 24286297 2013
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0004153
Disease:
Atherosclerosis
0.030 GeneticVariation BEFREE In the present study, we aimed to examine the role of two single-nucleotide polymorphisms (SNPs), rs3825807 and rs11556924, located in the ADAMTS7 and ZC3HC1 genes, respectively, associated with CAD in published GWASs in European populations and their possible contribution to the development of coronary atherosclerosis and cerebral LA atherosclerosis in a case-control study of an the Iranian population. 31679296 2019
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0003850
Disease:
Arteriosclerosis
0.030 GeneticVariation BEFREE In the present study, we aimed to examine the role of two single-nucleotide polymorphisms (SNPs), rs3825807 and rs11556924, located in the ADAMTS7 and ZC3HC1 genes, respectively, associated with CAD in published GWASs in European populations and their possible contribution to the development of coronary atherosclerosis and cerebral LA atherosclerosis in a case-control study of an the Iranian population. 31679296 2019
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0003850
Disease:
Arteriosclerosis
0.030 GeneticVariation BEFREE The resulting amino acid change Arg363His is associated with increased expression and nuclear mobility, as well as lower rates of cell growth in HeLa cells, further supporting a role for cell proliferation in atherosclerosis and its clinical consequences. 28115489 2017
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0004153
Disease:
Atherosclerosis
0.030 GeneticVariation BEFREE The resulting amino acid change Arg363His is associated with increased expression and nuclear mobility, as well as lower rates of cell growth in HeLa cells, further supporting a role for cell proliferation in atherosclerosis and its clinical consequences. 28115489 2017
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0003850
Disease:
Arteriosclerosis
0.030 GeneticVariation BEFREE Our results indicate that ZC3HC1 rs11556924 polymorphism is associated with subclinical atherosclerosis in RA. 24286297 2013
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0004153
Disease:
Atherosclerosis
0.030 GeneticVariation BEFREE Our results indicate that ZC3HC1 rs11556924 polymorphism is associated with subclinical atherosclerosis in RA. 24286297 2013
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C1314691
Disease:
Age at menarche
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0427460
Disease:
Red cell distribution width determination
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0007222
Disease:
Cardiovascular Diseases
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs56179563
rs56179563
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0200638
Disease:
Eosinophil count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0428883
Disease:
Diastolic blood pressure
C 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0871470
Disease:
Systolic Pressure
T 0.700 GeneticVariation GWASCAT The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. 27618452 2016
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0032181
Disease:
Platelet Count measurement
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0200641
Disease:
Blood basophil count (lab test)
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0428883
Disease:
Diastolic blood pressure
T 0.700 GeneticVariation GWASCAT The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. 27618452 2016
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0027051
Disease:
Myocardial Infarction
C 0.700 GeneticVariation GWASCAT A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. 26343387 2015
dbSNP: rs11556924
rs11556924
Entrez Id: 51530
Gene Symbol: ZC3HC1
ZC3HC1
CUI: C0038454
Disease:
Cerebrovascular accident
0.700 GeneticVariation GWASCAT Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325 2014