Entrez Id: |
3046 |
Gene Symbol: |
HBE1 |
HBE1
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.
|
26366553 |
2015 |
Entrez Id: |
53335 |
Gene Symbol: |
BCL11A |
BCL11A
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease.
|
27022141 |
2016 |
Entrez Id: |
3048 |
Gene Symbol: |
HBG2 |
HBG2
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |
Entrez Id: |
3048 |
Gene Symbol: |
HBG2 |
HBG2
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
|
20018918 |
2010 |
Entrez Id: |
53335 |
Gene Symbol: |
BCL11A |
BCL11A
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.
|
21326311 |
2011 |
Entrez Id: |
10767 |
Gene Symbol: |
HBS1L |
HBS1L
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.
|
26366553 |
2015 |
Entrez Id: |
10767 |
Gene Symbol: |
HBS1L |
HBS1L
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.
|
17767159 |
2007 |
Entrez Id: |
3046 |
Gene Symbol: |
HBE1 |
HBE1
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |
Entrez Id: |
3046 |
Gene Symbol: |
HBE1 |
HBE1
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
|
20018918 |
2010 |
Entrez Id: |
53335 |
Gene Symbol: |
BCL11A |
BCL11A
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.
|
25372704 |
2014 |
Entrez Id: |
282763 |
Gene Symbol: |
OR51B5 |
OR51B5
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
|
20018918 |
2010 |
Entrez Id: |
390058 |
Gene Symbol: |
OR51B6 |
OR51B6
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
|
20018918 |
2010 |
Entrez Id: |
53335 |
Gene Symbol: |
BCL11A |
BCL11A
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |
Entrez Id: |
3048 |
Gene Symbol: |
HBG2 |
HBG2
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.
|
26366553 |
2015 |
Entrez Id: |
4163 |
Gene Symbol: |
MCC |
MCC
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.
|
21326311 |
2011 |
Entrez Id: |
53335 |
Gene Symbol: |
BCL11A |
BCL11A
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.
|
17767159 |
2007 |
Entrez Id: |
53335 |
Gene Symbol: |
BCL11A |
BCL11A
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.
|
26366553 |
2015 |
Entrez Id: |
53335 |
Gene Symbol: |
BCL11A |
BCL11A
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
|
20018918 |
2010 |
Entrez Id: |
143630 |
Gene Symbol: |
UBQLNL |
UBQLNL
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |
Entrez Id: |
3050 |
Gene Symbol: |
HBZ |
HBZ
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |
Entrez Id: |
53335 |
Gene Symbol: |
BCL11A |
BCL11A
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.
|
21326311 |
2011 |
Entrez Id: |
3046 |
Gene Symbol: |
HBE1 |
HBE1
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans.
|
22936743 |
2012 |
Entrez Id: |
119696 |
Gene Symbol: |
OR51N1P |
OR51N1P
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |
Entrez Id: |
63935 |
Gene Symbol: |
PCIF1 |
PCIF1
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |
Entrez Id: |
85363 |
Gene Symbol: |
TRIM5 |
TRIM5
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |