Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8091
Gene Symbol: HMGA2
HMGA2
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A common variant of HMGA2 is associated with adult and childhood height in the general population. 17767157

2007
Entrez Id: 26137
Gene Symbol: ZBTB20
ZBTB20
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A common variant of HMGA2 is associated with adult and childhood height in the general population. 17767157

2007
Entrez Id: 2768
Gene Symbol: GNA12
GNA12
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 155185
Gene Symbol: AMZ1
AMZ1
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 129563
Gene Symbol: DIS3L2
DIS3L2
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 3479
Gene Symbol: IGF1
IGF1
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 4052
Gene Symbol: LTBP1
LTBP1
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 253461
Gene Symbol: ZBTB38
ZBTB38
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 105369942
Gene Symbol: LINC02456
LINC02456
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 517
Gene Symbol: ATP5MC2
ATP5MC2
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 5324
Gene Symbol: PLAG1
PLAG1
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 169714
Gene Symbol: QSOX2
QSOX2
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 1588
Gene Symbol: CYP19A1
CYP19A1
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 2202
Gene Symbol: EFEMP1
EFEMP1
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936

2010
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. 19570815

2009
Entrez Id: 129563
Gene Symbol: DIS3L2
DIS3L2
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. 19570815

2009
Entrez Id: 1021
Gene Symbol: CDK6
CDK6
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. 19570815

2009
Entrez Id: 23112
Gene Symbol: TNRC6B
TNRC6B
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. 19570815

2009
Entrez Id: 220107
Gene Symbol: DLEU7
DLEU7
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. 19570815

2009
Entrez Id: 5324
Gene Symbol: PLAG1
PLAG1
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. 19396169

2009
Entrez Id: 253461
Gene Symbol: ZBTB38
ZBTB38
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. 19396169

2009
Entrez Id: 2202
Gene Symbol: EFEMP1
EFEMP1
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. 19396169

2009
Entrez Id: 8200
Gene Symbol: GDF5
GDF5
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB Common variants in the GDF5-UQCC region are associated with variation in human height. 18193045

2008