|
C-reactive protein measurement
|
|
0.700 |
GeneticVariation
|
GWASDB |
New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis.
|
24763700 |
2014 |
|
C-reactive protein measurement
|
|
0.700 |
GeneticVariation
|
GWASDB |
Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore?
|
23844046 |
2013 |
|
C-reactive protein measurement
|
|
0.700 |
GeneticVariation
|
GWASDB |
Gene-centric analysis identifies variants associated with interleukin-6 levels and shared pathways with other inflammation markers.
|
23505291 |
2013 |
|
C-reactive protein measurement
|
|
0.700 |
GeneticVariation
|
GWASDB |
Genome-wide association with C-reactive protein levels in CLHNS: evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment.
|
21647738 |
2012 |
|
C-reactive protein measurement
|
|
0.700 |
GeneticVariation
|
GWASDB |
A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.
|
22291609 |
2012 |
|
Mental Depression
|
|
0.040 |
GeneticVariation
|
BEFREE |
Furthermore, we also identified some certain inherited CRP SNPs (A allele in rs1417938 and C allele in rs1205) could up regulate serum CRP level and distributed more in depression patients with family history.
|
30048584 |
2018 |
|
Depressed mood
|
|
0.040 |
GeneticVariation
|
BEFREE |
Furthermore, we also identified some certain inherited CRP SNPs (A allele in rs1417938 and C allele in rs1205) could up regulate serum CRP level and distributed more in depression patients with family history.
|
30048584 |
2018 |
|
Depressive disorder
|
|
0.040 |
GeneticVariation
|
BEFREE |
Furthermore, we also identified some certain inherited CRP SNPs (A allele in rs1417938 and C allele in rs1205) could up regulate serum CRP level and distributed more in depression patients with family history.
|
30048584 |
2018 |
|
Depressive disorder
|
|
0.040 |
GeneticVariation
|
BEFREE |
Furthermore, we also identified certain inherited CRP SNPs (A allele in rs1417938 and C allele in rs1205) which could up-regulate serum CRP levels and thus be associated with depression occurrence.
|
29340226 |
2017 |
|
Mental Depression
|
|
0.040 |
GeneticVariation
|
BEFREE |
Furthermore, we also identified certain inherited CRP SNPs (A allele in rs1417938 and C allele in rs1205) which could up-regulate serum CRP levels and thus be associated with depression occurrence.
|
29340226 |
2017 |
|
Depressed mood
|
|
0.040 |
GeneticVariation
|
BEFREE |
Furthermore, we also identified certain inherited CRP SNPs (A allele in rs1417938 and C allele in rs1205) which could up-regulate serum CRP levels and thus be associated with depression occurrence.
|
29340226 |
2017 |
|
Depressive disorder
|
|
0.040 |
GeneticVariation
|
BEFREE |
CRP gene variants were associated with serum levels in a gender-specific manner, but only rs1205 was found to be nominally associated with both an increased risk of DEP and lower circulating CRP levels in women.
|
25603415 |
2015 |
|
Depressed mood
|
|
0.040 |
GeneticVariation
|
BEFREE |
CRP gene variants were associated with serum levels in a gender-specific manner, but only rs1205 was found to be nominally associated with both an increased risk of DEP and lower circulating CRP levels in women.
|
25603415 |
2015 |
|
Mental Depression
|
|
0.040 |
GeneticVariation
|
BEFREE |
CRP gene variants were associated with serum levels in a gender-specific manner, but only rs1205 was found to be nominally associated with both an increased risk of DEP and lower circulating CRP levels in women.
|
25603415 |
2015 |
|
Depressive disorder
|
|
0.040 |
GeneticVariation
|
BEFREE |
Instead, we found that the risk of depression was greater amongst people who carry the rs1205 G > A genetic polymorphism of the CRP gene, which was associated with approximately 20% lower serum concentration of CRP compared with other genotypes.
|
19433520 |
2009 |
|
Depressed mood
|
|
0.040 |
GeneticVariation
|
BEFREE |
Instead, we found that the risk of depression was greater amongst people who carry the rs1205 G > A genetic polymorphism of the CRP gene, which was associated with approximately 20% lower serum concentration of CRP compared with other genotypes.
|
19433520 |
2009 |
|
Mental Depression
|
|
0.040 |
GeneticVariation
|
BEFREE |
Instead, we found that the risk of depression was greater amongst people who carry the rs1205 G > A genetic polymorphism of the CRP gene, which was associated with approximately 20% lower serum concentration of CRP compared with other genotypes.
|
19433520 |
2009 |
|
Ischemic stroke
|
|
0.030 |
GeneticVariation
|
BEFREE |
The adjusted odds ratios (ORs) [95% confidence interval (95% CI)] of IS per addition of the modelled allele were 1.07 (0.79-1.45) for rs876537, 0.99 (0.73-1.35) for rs1205 and 1.08 (0.71-1.65) for rs3093059.
|
31692152 |
2020 |
|
Ischemic stroke
|
|
0.030 |
GeneticVariation
|
BEFREE |
We found that rs2794521, rs3093059, and rs1205 were associated with decreased IS risk; we also found that gene-gene interaction between rs2794521 and rs3093059, and gene-environment interaction between rs2794521 and smoking were associated with decreased IS risk.
|
28287042 |
2017 |
|
Ischemic stroke
|
|
0.030 |
GeneticVariation
|
BEFREE |
Japanese patients with IS (72.4 +/- 8.2 years of age, n = 152) and elderly Japanese subjects without IS (78.0 +/- 4.2 years of age, n = 304) were genotyped for four SNP of the human CRP gene: rs1341665, rs1800947, rs1130864, and rs1205.
|
16733231 |
2006 |
|
Adenoma
|
|
0.020 |
GeneticVariation
|
BEFREE |
At rs1205 in CRP, T (minor allele) carriers had a higher risk (OR 1.67, 95%CI 1.07-2.60; reference: CC) of adenomas overall and adenomas with aggressive characteristics.
|
29802748 |
2018 |
|
Malignant neoplasm of breast
|
|
0.020 |
GeneticVariation
|
BEFREE |
We previously showed the association between C-reactive protein (CRP) 1846C>T (rs1205) polymorphism and LN metastasis in esophageal, non-small cell lung, and breast cancers.
|
26310275 |
2015 |
|
Malignant neoplasm of breast
|
|
0.020 |
GeneticVariation
|
BEFREE |
Among premenopausal AA women, comparing variant allele carriers to non-carriers, reduced breast cancer risk was associated with CXCL5-rs425535 (OR=0.61, P=0.02), while among EA women, there were associations with TNFA-rs1799724 (OR =2.31, P =0.002) and CRP-rs1205 (OR=0.54, P=0.01).
|
23991131 |
2013 |
|
Adenoma
|
|
0.020 |
GeneticVariation
|
BEFREE |
The C allele of rs1205 and the A allele of rs1130864 were significantly associated with higher serum CRP levels (p (trend): 0.0002 and 0.01, respectively), as well as with a decreased adenoma risk [rs1205: OR for CT and CC vs. TT = 0.69 (95% CI: 0.48-0.98) and 0.53 (0.34-0.83), respectively, p (trend) = 0.008; rs1130864: OR for GA and AA versus GG = 0.65 (0.45-0.93) and 0.74 (0.31-1.76), respectively, p (trend) = 0.04].
|
20333461 |
2010 |
|
Sepsis
|
|
0.010 |
GeneticVariation
|
BEFREE |
There was also a difference in CRP SNP rs1</span>205 between infants with septic shock and healthy infants, and between infants with septic shock and infants with sepsis.
|
29379005 |
2018 |