Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1126647
rs1126647
CUI: C0004936
Disease: Mental disorders
Mental disorders
0.010 GeneticVariation BEFREE In the present study, we genotyped three single nucleotide polymorphisms (SNPs) within IL-8 gene (rs4073, rs2227306 and rs1126647) in 229 individuals who attempted suicide with soft suicide methods, 235 suicide victims and 290 individuals without any history of psychiatric disorders or suicide attempt. 30099207

2018

dbSNP: rs1126647
rs1126647
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE The A T A haplotype (rs4073, rs2227306 and rs112</span>6647 respectively) was less frequent in PCa group compared with BPH group (OR (95% CI) = 0.4 (0.22-0.75), adjusted P value = 0.03). 30641210

2019

dbSNP: rs1126647
rs1126647
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 GeneticVariation BEFREE The risk for hypertension was increased in the presence of the T allele in IL8 rs1126647 (OR = 1.69, 95 % CI = 1.07-2.67, P = 0.024). 26387812

2015

dbSNP: rs1126647
rs1126647
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 GeneticVariation BEFREE The male population carrying the homozygote TT genotype and T allele of rs4073, the homozygote CC genotype and C allele of rs2227306 and homozygote AA genotype and A allele of rs1126647 are more susceptible to sepsis, suggesting there is a protective effect in females carrying these genotypes and alleles respectively. 27642120

2016

dbSNP: rs1126647
rs1126647
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 GeneticVariation BEFREE In the present study, we genotyped three single nucleotide polymorphisms (SNPs) within IL-8 gene (rs4073, rs2227306 and rs1126647) in 229 individuals who attempted suicide with soft suicide methods, 235 suicide victims and 290 individuals without any history of psychiatric disorders or suicide attempt. 30099207

2018

dbSNP: rs1126647
rs1126647
CUI: C0243026
Disease: Sepsis
Sepsis
0.010 GeneticVariation BEFREE The male population carrying the homozygote TT genotype and T allele of rs4073, the homozygote CC genotype and C allele of rs2227306 and homozygote AA genotype and A allele of rs1126647 are more susceptible to sepsis, suggesting there is a protective effect in females carrying these genotypes and alleles respectively. 27642120

2016

dbSNP: rs1126647
rs1126647
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 GeneticVariation BEFREE The A T A haplotype (rs4073, rs2227306 and rs112</span>6647 respectively) was less frequent in PCa group compared with BPH group (OR (95% CI) = 0.4 (0.22-0.75), adjusted P value = 0.03). 30641210

2019

dbSNP: rs1126647
rs1126647
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
0.010 GeneticVariation BEFREE The A T A haplotype (rs4073, rs2227306 and rs112</span>6647 respectively) was less frequent in PCa group compared with BPH group (OR (95% CI) = 0.4 (0.22-0.75), adjusted P value = 0.03). 30641210

2019

dbSNP: rs2227306
rs2227306
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 GeneticVariation BEFREE Our data showed that the expression level of IL-8 was associated with the development of GD, and the C-allele frequency of SNP rs2227306 was significantly higher in GD and GO patients compared with healthy controls. 19816813

2009

dbSNP: rs2227306
rs2227306
CUI: C0004096
Disease: Asthma
Asthma
0.010 GeneticVariation BEFREE The presence of IL8-251 A/T (rs4073) and + 781C/T (rs2227306) polymorphisms was significantly associated with an increased risk of asthma (P = 0.002, P = 0.036, respectively). 28993876

2017

dbSNP: rs2227306
rs2227306
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
0.010 GeneticVariation BEFREE The A T A haplotype (rs4073, rs2227306 and rs1126647 respectively) was less frequent in PCa group compared with BPH group (OR (95% CI) = 0.4 (0.22-0.75), adjusted P value = 0.03). 30641210

2019

dbSNP: rs2227306
rs2227306
CUI: C0024115
Disease: Lung diseases
Lung diseases
0.010 GeneticVariation BEFREE The severity of lung disease was associated with the following markers: transcutaneous arterial hemoglobin oxygen saturation (SaO2) (regardless of CFTR genotype, for the polymorphisms rs4073, rs2227306 and rs2227307); mucoid Pseudomonas aeruginosa (regardless of CFTR genotype, for the polymorphisms rs2227306 and rs2227307). 27209008

2016

dbSNP: rs2227306
rs2227306
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE The A T A haplotype (rs4073, rs2227306 and rs1126647 respectively) was less frequent in PCa group compared with BPH group (OR (95% CI) = 0.4 (0.22-0.75), adjusted P value = 0.03). 30641210

2019

dbSNP: rs2227306
rs2227306
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.010 GeneticVariation BEFREE The aim of the current study was to examine the influence of the IL-8 gene polymorphisms at positions -251 (rs4073) and +781 (rs2227306) on the risk of osteoarthritis. 25194757

2014

dbSNP: rs2227306
rs2227306
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.010 GeneticVariation BEFREE This study identified the IL8 gene, represented by rs4073 and rs2227306 polymorphisms, and particularly the rs2227307 polymorphism, as potentiating factors for the degree of variability in the severity of CF, especially in pulmonary clinical manifestation correlated with increased morbidity and mortality. 27209008

2016

dbSNP: rs2227306
rs2227306
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.010 GeneticVariation BEFREE However, we observed no significant relationship between the IL-8 rs2227306 polymorphism and primary gouty arthritis risk. 27813564

2016

dbSNP: rs2227306
rs2227306
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 GeneticVariation BEFREE The male population carrying the homozygote TT genotype and T allele of rs4073, the homozygote CC genotype and C allele of rs22</span>27306 and homozygote AA genotype and A allele of rs1126647 are more susceptible to sepsis, suggesting there is a protective effect in females carrying these genotypes and alleles respectively. 27642120

2016

dbSNP: rs2227306
rs2227306
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 GeneticVariation BEFREE Two IL8 SNPs (rs4073A/T, rs2227306C/T) and three SNPs tagging CXCR1 and CXCR2 (rs4674258C/T, rs1008563C/T, rs6723449T/C) were analyzed for association with IL8 levels and with MI risk. 24462138

2014

dbSNP: rs2227306
rs2227306
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 GeneticVariation BEFREE The A T A haplotype (rs4073, rs2227306 and rs1126647 respectively) was less frequent in PCa group compared with BPH group (OR (95% CI) = 0.4 (0.22-0.75), adjusted P value = 0.03). 30641210

2019

dbSNP: rs2227306
rs2227306
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.010 GeneticVariation BEFREE One promoter (rs4073T>A) and two intronic SNPs (rs2227307T>G and rs2227306C>T) of the IL-8 genes were genotyped in 237 subjects with IPF and 456 normal controls. 21649933

2011

dbSNP: rs2227306
rs2227306
Liver and Intrahepatic Biliary Tract Carcinoma
0.010 GeneticVariation BEFREE Our objective was to examine the association between single nucleotide polymorphisms of interleukin (IL)-8 (rs4073 and rs2227306) and IL-10 (rs1800871 and rs1800872) genes, and clinical effects of transcatheter arterial chemoembolization (TACE) and subsequent prognosis in patients with liver cancer. 26400525

2015

dbSNP: rs2227306
rs2227306
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 GeneticVariation BEFREE The genotyping data from 192 patients with childhood IgAN and 397 controls showed significant differences in the frequencies of the CXCL8 gene with rs2227306 (dominant, P = 0.019; overdominant, P = 0.009), rs2227543 (dominant, P = 0.01; overdominant, P = 0.0057), and rs4073 (codominant, P = 0.034; dominant, P = 0.011; overdominant, P = 0.022). 21214373

2011

dbSNP: rs2227306
rs2227306
CUI: C0206139
Disease: Lichen Planus, Oral
Lichen Planus, Oral
0.010 GeneticVariation BEFREE Four SNPs of the IL-8 gene at positions -845 T/C (rs2227532), -738 T/A, -251 A/T (rs4073) and +781 C/T (rs2227306) were analyzed in 109 patients with OLP and 101 normal controls using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. 19842025

2010

dbSNP: rs2227306
rs2227306
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver
0.010 GeneticVariation BEFREE Our objective was to examine the association between single nucleotide polymorphisms of interleukin (IL)-8 (rs4073 and rs2227306) and IL-10 (rs1800871 and rs1800872) genes, and clinical effects of transcatheter arterial chemoembolization (TACE) and subsequent prognosis in patients with liver cancer. 26400525

2015

dbSNP: rs2227306
rs2227306
CUI: C0017638
Disease: Glioma
Glioma
0.010 GeneticVariation BEFREE In conclusion, we determined that there is a lack of evidence suggesting a significant association between the IL-8 rs4073 and rs2227306 gene polymorphisms and the development of glioma in a Chinese population. 27706570

2016