Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1061170
rs1061170
CFH
0.020 GeneticVariation BEFREE Serum complement factor H and Tyr402 His gene polymorphism among Egyptians with multiple sclerosis. 26186240

2015
dbSNP: rs1061170
rs1061170
CFH
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