CXCL11, C-X-C motif chemokine ligand 11, 6373

N. diseases: 164; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4619915
rs4619915
Entrez Id: 419;6373
Gene Symbol: ART3;CXCL11
ART3;CXCL11
CUI: C0019196
Disease:
Hepatitis C
0.020 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: rs4619915
rs4619915
Entrez Id: 419;6373
Gene Symbol: ART3;CXCL11
ART3;CXCL11
CUI: C0019196
Disease:
Hepatitis C
0.020 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
dbSNP: rs4619915
rs4619915
Entrez Id: 419;6373
Gene Symbol: ART3;CXCL11
ART3;CXCL11
CUI: C0239946
Disease:
Fibrosis, Liver
0.010 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: rs4619915
rs4619915
Entrez Id: 419;6373
Gene Symbol: ART3;CXCL11
ART3;CXCL11
CUI: C3854222
Disease:
Human immunodeficiency virus (HIV) II infection category B1
0.010 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: rs6817952
rs6817952
Entrez Id: 419;6373
Gene Symbol: ART3;CXCL11
ART3;CXCL11
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
0.010 GeneticVariation BEFREE CXCL11 rs6817952 nucleotide substitution was determined in 501 German individuals with IBD (336 CD, 165 UC) including 258 children and 243 adults as well as in 231 controls by a TaqMan SNP genotyping assay. 20848514 2010