Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3921
rs3921
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.030 GeneticVariation BEFREE Here we recruited chronic hepatitis C (CHC) patients to perform an association study between three single nucleotide polymorphisms (SNPs) (CXCR2 rs1126579, CXCL10 rs8878 and CXCL10 rs3921) and HCV infection outcomes and treatment responses among a Chinese population, using primarily a TaqMan assay. 29948377

2018

dbSNP: rs3921
rs3921
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.030 GeneticVariation BEFREE The homozygosity for the minor alleles CXCL9 rs10336 (T), CXCL10 rs3921 (G), and CXCL11 rs4619915 (A) is associated with the higher likelihood of significant liver fibrosis in HIV-infected patients coinfected with HCV-GT1. 25559603

2015

dbSNP: rs3921
rs3921
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.030 GeneticVariation BEFREE The presence of homozygous for the minor allele of CXCL9 rs10336, CXCL10 rs3921 and CXCL11 rs4619915 was related to higher likelihoods of achieving the HCV clearance after pegIFNα/ribavirin therapy in HIV infected patients coinfected with HCV GT1/4. 25218243

2014