CX3CL1, C-X3-C motif chemokine ligand 1, 6376

N. diseases: 243; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62037084
rs62037084
Entrez Id: 6376
Gene Symbol: CX3CL1
CX3CL1
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs671623
rs671623
Entrez Id: 6376
Gene Symbol: CX3CL1
CX3CL1
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs8102
rs8102
Entrez Id: 6376
Gene Symbol: CX3CL1
CX3CL1
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs170364
rs170364
Entrez Id: 6376
Gene Symbol: CX3CL1
CX3CL1
CUI: C1956346
Disease:
Coronary Artery Disease
0.020 GeneticVariation BEFREE CX3CL1 and CX3CR1 may contribute to the formation of coronary atherosclerotic plaque in CAD.CX3CL1 rs170364 and CX3CR1 rs17793056 polymorphisms may be independent genetic risk factors for CAD. 25845619 2015
dbSNP: rs170364
rs170364
Entrez Id: 6376
Gene Symbol: CX3CL1
CX3CL1
CUI: C1956346
Disease:
Coronary Artery Disease
0.020 GeneticVariation BEFREE No significant correlation was found between T allele of rs170364 and CAD risk (P>0.05). 26191329 2015
dbSNP: rs614230
rs614230
Entrez Id: 6376
Gene Symbol: CX3CL1
CX3CL1
CUI: C0150055
Disease:
Chronic pain
0.010 GeneticVariation BEFREE We analyzed the CCL2 gene rs4586, CALCA rs3781719, CX3CL1 rs614230 single nucleotide polymorphism (SNPs) of 350 Chinese Han women with chronic postsurgical pain (CPSP) 6 months after cesarean section and 350 healthy women without chronic pain (HC). 31441843 2019
dbSNP: rs148601459
rs148601459
Entrez Id: 6376
Gene Symbol: CX3CL1
CX3CL1
CUI: C0009324
Disease:
Ulcerative Colitis
0.010 GeneticVariation BEFREE Genotypes of fractalkine receptorc.745G>A (V249I) and c.839C>T (T280M) polymorphisms were identified by restriction fragment length polymorphism analyses after polymerase chain reaction.Genotype distribution and allele frequencies of V249I and T280M were not statistically significantly different between UC and control groups (p>0.05). 26042517 2015
dbSNP: rs614230
rs614230
Entrez Id: 6376
Gene Symbol: CX3CL1
CX3CL1
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE CC genotype and C allele in rs614230 (CX3CL1) were significantly related with decreased risk of CAD (OR=0.38, 95% CI=0.17-0.86; OR=0.66, 95% CI=0.45-0.97).For IL-6 rs2066992 polymorphism. 26191329 2015
dbSNP: rs148601459
rs148601459
Entrez Id: 6376
Gene Symbol: CX3CL1
CX3CL1
CUI: C0149517
Disease:
Chronic tonsillitis
0.010 GeneticVariation BEFREE Genotypes were identified by restriction fragment length polymorphism analyses after polymerase chain reaction. c.745G>A (V249I) single nucleotide polymorphism and the frequencies of the G and A alleles did not differ in the patient and control groups (p = 0.363; p = 0.743, respectively). c.839C>T (T280M) single nucleotide polymorphism was found to be higher in controls than in the patients with chronic tonsillitis (p < 0.001). 24496565 2014