rs4858647, None

N. diseases: 2
Disease: Primary Myelofibrosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
0.010 GeneticVariation BEFREE THRB-RARB rs4858647 had a weak association with PMF only (OR = 1.5; 95% CI = 1-2.1; P-value = .04). 29047144 2018