rs6051702, C20orf194

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Anemia
CUI: C0002871
Disease: Anemia
0.040 GeneticVariation BEFREE Polymorphisms of inosine triphosphate pyrophosphatase (rs1127354 and rs6051702) and interferon lambda 4 (IFLN4) (rs12979860) are indicators of anemia and/or sustained virological response (SVR) in patients with chronic hepatitis C on ribavirin/interferon. 31359493 2020
Anemia
CUI: C0002871
Disease: Anemia
0.040 GeneticVariation BEFREE Baseline testing of rs6051702 may identify the subset of patients at greatest risk for RBV-induced anaemia using interferon-free hepatitis C therapies. 28198349 2017
Anemia
CUI: C0002871
Disease: Anemia
0.040 GeneticVariation BEFREE The ITPA rs1127354 CC and rs6051702 AA genotypes may predict ribavirin-induced anemia during treatment with interferon-free, ribavirin-containing regimens. 26650626 2015
Anemia
CUI: C0002871
Disease: Anemia
0.040 GeneticVariation BEFREE In multivariate logistic regression analyses the carrier of a variant allele in the rs6051702/rs1127354 association (OR=0.11, p=1.75×10(-5)) and Hb at baseline (OR=1.51, p=1.21×10(-4)) were independently associated with protection against clinically significant anemia at week 4. 23933495 2013