rs1205
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;T) | 0 | common in complete genomics |
Make rs1205(C;C) |
Make rs1205(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 159712443 |
Gene | CRP |
is a | snp |
is | mentioned by |
dbSNP | rs1205 |
dbSNP (classic) | rs1205 |
ClinGen | rs1205 |
ebi | rs1205 |
HLI | rs1205 |
Exac | rs1205 |
Gnomad | rs1205 |
Varsome | rs1205 |
LitVar | rs1205 |
Map | rs1205 |
PheGenI | rs1205 |
Biobank | rs1205 |
1000 genomes | rs1205 |
hgdp | rs1205 |
ensembl | rs1205 |
geneview | rs1205 |
scholar | rs1205 |
rs1205 | |
pharmgkb | rs1205 |
gwascentral | rs1205 |
openSNP | rs1205 |
23andMe | rs1205 |
SNPshot | rs1205 |
SNPdbe | rs1205 |
MSV3d | rs1205 |
GWAS Ctlg | rs1205 |
GMAF | 0.365 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Although somewhat lacking in statistical power, several reports have linked rs1205, a UTR mutation known as CRP4 in the C-reactive protein CRP to the autoimmune disorder SLE, systemic lupus erythematosus. The risk allele in dbSNP orientation is (T). [PMID 14645206, PMID 15897982]
[PMID 19139754] C-reactive protein (CRP) levels obesity rs1205(G) allele had significantly higher CRP levels than noncarriers in a dose-dependent manner suggesting a possible association with fat localization
23andMe blog each rs1205(T) lowered CRP by 20% but no association with heart disease.
[PMID 19040303] C-reactive protein gene polymorphisms in biopsy-proven giant cell arteritis from Northwestern Spain
[PMID 19433520] Polymorphisms of the CRP gene inhibit inflammatory response and increase susceptibility to depression: The Health in Men Study
[PMID 19101671] Association between C-reactive protein gene haplotypes and C-reactive protein levels in Taiwanese: interaction with obesity
[PMID 19692124] Complement Factor H Y402H and C-Reactive Protein Polymorphism and Photodynamic Therapy Response in Age-Related Macular Degeneration
[PMID 19821022] Genetic variants associated with altered plasma levels of C-reactive protein are not associated with late-life cognitive ability in four Scottish samples
[PMID 19965533] CRP polymorphisms and progression of chronic kidney disease in African Americans
[PMID 20538124] Genetic Polymorphisms and the Cardiovascular Risk of Non-Steroidal Anti-Inflammatory Drugs
[PMID 20552244] Genetic polymorphism of the C-reactive protein (CRP) gene and a deep infection focus determine maximal serum CRP level in Staphylococcus aureus bacteremia
[PMID 20733302] Genetic Variants in the C-Reactive Protein Gene Are Associated with Microangiopathic Ischemic Stroke
[PMID 20333461] Serum CRP and IL-6, genetic variants and risk of colorectal adenoma in a multiethnic population
[PMID 20856253] Combined effect of C-reactive protein gene SNP +2147 A/G and interleukin-6 receptor gene SNP rs2229238 C/T on anthropometric characteristics among school children in Taiwan
[PMID 20949557] Genetic variation in C-reactive protein (CRP) in relation to colon and rectal cancer risk and survival
[PMID 21293934] Association of C-reactive Protein Gene Polymorphisms and Colorectal Cancer
[PMID 21413847] Polymorphism in the C-reactive protein (CRP) gene affects CRP levels in plasma and one early marker of atherosclerosis in men: The Health 2000 Survey
[PMID 21080913] The CRP genotype, serum levels and lung function in men: the Caerphilly Prospective Study
[PMID 21575917] C reactive protein and alpha1-antitrypsin: relationship between levels and gene variants
[PMID 22004660] Genetic Variants, Immune Function, and Risk of Pre-Eclampsia among American Indians
[PMID 16519819] Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases.
[PMID 16723442] A prospective assessment of the Y402H variant in complement factor H, genetic variants in C-reactive protein, and risk of age-related macular degeneration.
[PMID 16733231] Association study between C-reactive protein genes and ischemic stroke in Japanese subjects.
[PMID 16820586] Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.
[PMID 16832152] Polymorphism of the C-reactive protein (CRP) gene is related to serum CRP Level and arterial pulse wave velocity in healthy elderly Japanese.
[PMID 17101857] Genetic variation is associated with C-reactive protein levels in the Third National Health and Nutrition Examination Survey.
[PMID 17697822] Usefulness of combining complement factor H and C-reactive protein genetic profiles for predicting myocardial infarction (from the Rotterdam Study).
[PMID 17888441] Common variants in the CRP gene in relation to longevity and cause-specific mortality in older adults: the Cardiovascular Health Study.
[PMID 17900590] C-reactive protein gene variation and type 2 diabetes mellitus: a case-control study.
[PMID 17903293] Genome-wide association with select biomarker traits in the Framingham Heart Study.
[PMID 17956875] DNA variants, plasma levels and variability of C-reactive protein in myocardial infarction survivors: results from the AIRGENE study.
[PMID 18000615] Common haplotypes of the C-reactive protein gene and circulating leptin levels influence the interindividual variability in serum C-reactive protein levels. The Segovia study.
[PMID 18162041] Neovascular age-related macular degeneration risk based on CFH, LOC387715/HTRA1, and smoking.
[PMID 18167554] C-reactive protein (CRP) gene polymorphisms, CRP levels, and risk of incident coronary heart disease in two nested case-control studies.
[PMID 18216863] Genetic determinants of basal C-reactive protein expression in Filipino systemic lupus erythematosus families.
[PMID 18285551] Association of common C-reactive protein (CRP) gene polymorphisms with baseline plasma CRP levels and fenofibrate response: the GOLDN study.
[PMID 18385179] Systemic inflammation, genetic susceptibility and lung function.
[PMID 18394581] Bayesian meta-analysis of genetic association studies with different sets of markers.
[PMID 18439548] Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.
[PMID 18500540] Fine-mapping the genetic basis of CRP regulation in African Americans: a Bayesian approach.
[PMID 18700811] Inflammation, insulin resistance, and diabetes--Mendelian randomization using CRP haplotypes points upstream.
[PMID 18704199] Comprehensive analysis of CRP, CFH Y402H and environmental risk factors on risk of neovascular age-related macular degeneration.
[PMID 18714381] Does high C-reactive protein concentration increase atherosclerosis? The Whitehall II Study.
[PMID 18714384] The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4,610 cases amongst 18,637 participants.
[PMID 18793001] Genetic variation in C-reactive protein (CRP) gene may be associated with risk of systemic lupus erythematosus and CRP concentrations.
[PMID 19075099] Association between C-reactive protein genotype, circulating levels, and aortic pulse wave velocity.
[PMID 19076828] Genetics of C-reactive protein and complement factor H have an epistatic effect on carotid artery compliance: the Cardiovascular Risk in Young Finns Study.
[PMID 19095725] Relation of genetic variation in the gene coding for C-reactive protein with its plasma protein concentrations: findings from the Women's Health Initiative Observational Cohort.
[PMID 19262552] C-reactive protein polymorphisms and genetic susceptibility to ischemic stroke and hemorrhagic stroke in the Chinese Han population.
[PMID 19267250] C-reactive protein, interleukin-6, and prostate cancer risk in men aged 65 years and older.
[PMID 19272152] IL6 and CRP haplotypes are associated with COPD risk and systemic inflammation: a case-control study.
[PMID 19410251] Association of C-reactive protein (CRP) gene allelic variants with serum CRP levels and hypertension in Turkish adults.
[PMID 19426506] C-Reactive protein gene variants are associated with postoperative C-reactive protein levels after coronary artery bypass surgery.
[PMID 19436291] C-reactive protein haplotype is associated with high PSA as a marker of metastatic prostate cancer but not with overall cancer risk.
[PMID 19567438] Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease.
[PMID 19796676] Polymorphisms in the CRP gene moderate an association between depressive symptoms and circulating levels of C-reactive protein.
[PMID 19906786] Unraveling the directional link between adiposity and inflammation: a bidirectional Mendelian randomization approach.
[PMID 19962488] Pleiotropy of C-reactive protein gene polymorphisms with C-reactive protein levels and heart rate variability in healthy male twins.
[PMID 20078877] Gene polymorphisms in association with emerging cardiovascular risk markers in adult women.
[PMID 20616999] Usefulness of Mendelian randomization in observational epidemiology.
[PMID 20974458] Maternal C-reactive protein levels in pregnancy are associated with wheezing and lower respiratory tract infections in the offspring.
[PMID 21034294] C-reactive protein polymorphisms are associated with the cortisol awakening response in basal conditions in human subjects.
[PMID 21094359] Effect of central obesity, low high-density lipoprotein cholesterol and C-reactive protein polymorphisms on C-reactive protein levels during treatment with Rosuvastatin (10 mg Daily).
[PMID 21296145] Association between adolescent emotional problems and metabolic syndrome: the modifying effect of C-reactive protein gene (CRP) polymorphisms.
[PMID 21325005] Association between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant data.
[PMID 21647738] 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.
[PMID 21790705] The polymorphisms of C-reactive protein gene modify the association between central obesity and lung function in taiwan asthmatics.
[PMID 21979869] C-reactive protein haplotypes and dispositional optimism in obese and nonobese elderly subjects.
[PMID 23212764] Evaluation of the Risk of Lymph Node Metastasis Using CRP 1846C>T Genetic Polymorphism in Submucosal Thoracic Esophageal Squamous Cell Carcinoma
[PMID 23254959] Serum C-reactive protein and risk of lung cancer: a case-control study
[PMID 23267696] Association of genetic polymorphisms with chronic obstructive pulmonary disease in the Chinese Han population: a case-control study
[PMID 23940726] Two variants of the C-reactive protein gene are associated with risk of pre-eclampsia in an american Indian population
[PMID 24574329] Serum C-reactive protein (CRP) associates with lupus disease activity in the absence of measurable interferon alpha and a CRP gene variant
[PMID 24602049] Association of gene polymorphisms with the risk of warfarin bleeding complications at therapeutic INR in patients with mechanical cardiac valves
[PMID 23397258] Association study of CRP gene in systemic sclerosis in European Caucasian population.
[PMID 24862635] Association of CRP gene polymorphisms with serum CRP level and handgrip strength in community-dwelling elders in Taiwan: Taichung Community Health Study for Elders (TCHS-E)
[PMID 24894103] Serum C-reactive protein level but not its gene polymorphism is associated with Takayasu arteritis
[PMID 25025473] Mutations of C-Reactive Protein (CRP) -286 SNP, APC and p53 in Colorectal Cancer: Implication for a CRP-Wnt Crosstalk
[PMID 25020710] P324Circadian genes in the regulation of lipids in coronary artery disease
[PMID 25043606] Association of CRP genetic variants with blood concentrations of C-reactive protein and colorectal cancer risk
[PMID 25993353] Association of IL-6 and CRP gene polymorphisms with obesity and metabolic disorders in children and adolescents
[PMID 25224558] Association of variants in genes related to the immune response and obesity with BPH in CLUE II
[PMID 26310275] CRP 1846C>T Genetic Polymorphism Is Associated with Lymph Node Metastasis and/or Severe Lymphatic Invasion in Endometrial Cancer
[PMID 26456189] Interaction of SNP in the CRP gene and plasma fatty acid profile in inflammatory pattern: A cross-sectional population-based study
[PMID 26473826] Association of the C-Reactive Protein Gene (CRP) rs1205 C>T Polymorphism with Aortic Valve Calcification in Patients with Aortic Stenosis
[PMID 26550110] The role of gene variants of the inflammatory markers CRP and TNF-α in cardiovascular heart disease: systematic review and meta-analysis
[PMID 26813132] [Association of single nucleotide polymorphisms of IL-6 gene with longevity in Uyghurs in Xinjiang].
[PMID 27891353] Association of C-Reactive Protein (rs1205) Gene Polymorphism with Susceptibility to Psoriasis in South Indian Tamils.
[PMID 28287042] Impact of CRP gene and additional gene-smoking interaction on ischemic stroke in a Chinese Han population.
[PMID 29379005] Association of Single-Nucleotide Polymorphisms of C-Reactive Protein Gene with Susceptibility to Infantile Sepsis in Southern China.
[PMID 29556849] C-reactive protein (CRP) polymorphisms and haplotypes are associated with SLE susceptibility and activity but not with serum CRP levels in Mexican population.
[PMID 31500937] Interplay between the Mediterranean diet and C-reactive protein genetic polymorphisms towards inflammation in adolescents.
[PMID 31692152] Association of plasma C-reactive protein with ischemic stroke: A Mendelian randomization study.
[PMID 32514365] C-reactive protein gene rs1205 polymorphism is associated with low-grade chronic inflammation in postmenopausal women.
[PMID 33296257] The Genetic Variants -717T>C (rs2794521), 1444G>A (rs1130864), and 1846 C > T (rs1205) of CRP Gene, Their Haplotypes, and Their Association with Serum CRP Levels, Acute Coronary Syndrome, and Diabetes in Patients from Western Mexico.
- Is a snp
- In dbSNP
- SNPs on chromosome 1
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- Pages using PMID magic links