rs1061170, CFH

N. diseases: 72
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Chronic Fatigue Syndrome
CUI: C0015674
Disease: Chronic Fatigue Syndrome
0.010 GeneticVariation BEFREE Of particular interest is association of CFS with two missense variants in genes of complement activation, rs4151667 (L9H) in CFB and rs1061170 (Y402H) in CFH. 26116897 2015