rs1061170, CFH

N. diseases: 72
Disease: Multiple Sclerosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.020 GeneticVariation BEFREE Serum complement factor H and Tyr402 His gene polymorphism among Egyptians with multiple sclerosis. 26186240 2015
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.020 GeneticVariation BEFREE We examined whether the complement regulator factor H and its Tyr402His polymorphism, recently implicated as biomarkers in other chronic inflammatory central nervous system conditions, might identify or predict specific pathological processes and outcomes in multiple sclerosis. 20421219 2010