rs8007267, None

N. diseases: 6
Disease: Anemia, Sickle Cell ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
0.010 GeneticVariation BEFREE The presence of a GCH1 haplotype with high BH4 in populations of African ancestry could explain the association of rs8007267 with sickle cell anemia pain crises. 24136375 2014