Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs766432
rs766432
BCL11A
0.800 GeneticVariation GWASCAT Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease. 27022141

2016
dbSNP: rs766432
rs766432
BCL11A
0.800 GeneticVariation GWASDB Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans. 22936743

2012
dbSNP: rs766432
rs766432
BCL11A
0.800 GeneticVariation GWASDB Recently, BCL11A (zinc-finger protein) was identified as a regulator of HbF, and the strongest association signals were observed either directly for rs766432 or for correlated single-nucleotide polymorphisms (SNPs). 21326311

2011
dbSNP: rs766432
rs766432
BCL11A
0.800 GeneticVariation GWASCAT Recently, BCL11A (zinc-finger protein) was identified as a regulator of HbF, and the strongest association signals were observed either directly for rs766432 or for correlated single-nucleotide polymorphisms (SNPs). 21326311

2011
dbSNP: rs766432
rs766432
BCL11A
0.800 GeneticVariation GWASDB Genome-wide association studies also validated a previously identified SNP (rs766432) in BCL11A, a gene known to affect fetal hemoglobin levels (P = 2.6E-21) and in Thailand and Hong Kong subjects. 20018918

2010
dbSNP: rs766432
rs766432
BCL11A
C 0.800 GeneticVariation GWASCAT Genome-wide association studies also validated a previously identified SNP (rs766432) in BCL11A, a gene known to affect fetal hemoglobin levels (P = 2.6E-21) and in Thailand and Hong Kong subjects. 20018918

2010
dbSNP: rs766432
rs766432
BCL11A
0.800 GeneticVariation GWASDB A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. 17767159

2007