Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4036
Gene Symbol: LRP2
LRP2 		0.200 Biomarker disease MGD
Entrez Id: 6641
Gene Symbol: SNTB1
SNTB1 		0.100 GeneticVariation disease GWASCAT A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population. 23406873 2013
Entrez Id: 7434
Gene Symbol: VIPR2
VIPR2 		0.100 GeneticVariation disease GWASCAT A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population. 23406873 2013
Entrez Id: 6641
Gene Symbol: SNTB1
SNTB1 		0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia. 23933737 2013
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2 		0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia. 23933737 2013
Entrez Id: 6424
Gene Symbol: SFRP4
SFRP4 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 2313
Gene Symbol: FLI1
FLI1 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 5371
Gene Symbol: PML
PML 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 89795
Gene Symbol: NAV3
NAV3 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 5789
Gene Symbol: PTPRD
PTPRD 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 6711
Gene Symbol: SPTBN1
SPTBN1 		0.100 GeneticVariation disease GWASCAT Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. 22685421 2012
Entrez Id: 389432
Gene Symbol: SAMD5
SAMD5 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 1665
Gene Symbol: DHX15
DHX15 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 443
Gene Symbol: ASPA
ASPA 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 6733
Gene Symbol: SRPK2
SRPK2 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 84690
Gene Symbol: SPATA22
SPATA22 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 10579
Gene Symbol: TACC2
TACC2 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 399715
Gene Symbol: LINC02649
LINC02649 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 654
Gene Symbol: BMP6
BMP6 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 729305
Gene Symbol: LINC02714
LINC02714 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 26974
Gene Symbol: ZNF285
ZNF285 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 9745
Gene Symbol: ZNF536
ZNF536 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 64084
Gene Symbol: CLSTN2
CLSTN2 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
Entrez Id: 57706
Gene Symbol: DENND1A
DENND1A 		0.100 GeneticVariation disease GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012