Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4671393
rs4671393
BCL11A
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.710 GeneticVariation BEFREE rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients. 27077760

2016
dbSNP: rs4671393
rs4671393
BCL11A
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.710 GeneticVariation GWASCAT Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311

2011