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 |
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: |
282763 |
Gene Symbol: |
OR51B5 |
OR51B5
|
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 |
Entrez Id: |
390058 |
Gene Symbol: |
OR51B6 |
OR51B6
|
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 |
Entrez Id: |
53335 |
Gene Symbol: |
BCL11A |
BCL11A
|
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 |
Entrez Id: |
3046 |
Gene Symbol: |
HBE1 |
HBE1
|
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 |
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: |
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: |
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: |
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 |
Entrez Id: |
282763 |
Gene Symbol: |
OR51B5 |
OR51B5
|
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 |
GWASDB |
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
|
18245381 |
2008 |
Entrez Id: |
79300 |
Gene Symbol: |
OR51P1P |
OR51P1P
|
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: |
56547 |
Gene Symbol: |
MMP26 |
MMP26
|
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: |
79529 |
Gene Symbol: |
OR52J2P |
OR52J2P
|
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: |
119682 |
Gene Symbol: |
OR51L1 |
OR51L1
|
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: |
81285 |
Gene Symbol: |
OR51E2 |
OR51E2
|
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: |
401662 |
Gene Symbol: |
OR51A8P |
OR51A8P
|
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: |
143502 |
Gene Symbol: |
OR52I2 |
OR52I2
|
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: |
3042 |
Gene Symbol: |
HBM |
HBM
|
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: |
143425 |
Gene Symbol: |
SYT9 |
SYT9
|
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 |