rs1799864, CCR2

N. diseases: 68
Disease: Hepatitis C ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
0.040 GeneticVariation BEFREE Susceptibility to HCV infection is associated with A alleles of both (rs743660 and rs1799864 G/A) of CCR2 while spontaneous clearance of HCV is associated with the C allele of rs13900 of CCL2 and T allele of rs3817655 of CCL5. 30175654 2019
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
0.040 GeneticVariation BEFREE CCL2-2518 A/G and CCR2 190 A/G do not influence the outcome of hepatitis C virus infection in the Spanish population. 17465499 2007
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
0.040 GeneticVariation BEFREE The CCR2-V64I allele was present in 24 of 278 HCV chromosomes (8.6%) and 19 of 200 control chromosomes (9.5%). 15230854 2004
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
0.040 GeneticVariation BEFREE The G190A polymorphism (variant allele Ile64) in the first transmembrane domain of CCR2 was under-represented in the 29 patients who had cleared the hepatitis C virus spontaneously (P = 0.018). 15086398 2004