Entrez Id: |
81246 |
Gene Symbol: |
OR52Q1P |
OR52Q1P
|
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: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
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: |
8131 |
Gene Symbol: |
NPRL3 |
NPRL3
|
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: |
283110 |
Gene Symbol: |
OR52Z1 |
OR52Z1
|
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 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 |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |
Entrez Id: |
10767 |
Gene Symbol: |
HBS1L |
HBS1L
|
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: |
4676 |
Gene Symbol: |
NAP1L4 |
NAP1L4
|
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: |
3046 |
Gene Symbol: |
HBE1 |
HBE1
|
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: |
390063 |
Gene Symbol: |
OR51I1 |
OR51I1
|
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: |
81261 |
Gene Symbol: |
OR52H2P |
OR52H2P
|
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: |
81282 |
Gene Symbol: |
OR51G2 |
OR51G2
|
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: |
256892 |
Gene Symbol: |
OR51F1 |
OR51F1
|
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 |
GWASCAT |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |
Entrez Id: |
390059 |
Gene Symbol: |
OR51M1 |
OR51M1
|
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: |
81270 |
Gene Symbol: |
OR52B5P |
OR52B5P
|
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: |
101927763 |
Gene Symbol: |
OLFM5P |
OLFM5P
|
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: |
390082 |
Gene Symbol: |
OR52E5 |
OR52E5
|
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: |
3045 |
Gene Symbol: |
HBD |
HBD
|
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: |
6240 |
Gene Symbol: |
RRM1 |
RRM1
|
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: |
3043 |
Gene Symbol: |
HBB |
HBB
|
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: |
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: |
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: |
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: |
3048 |
Gene Symbol: |
HBG2 |
HBG2
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
|
20018918 |
2010 |