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: 399959
Gene Symbol: MIR100HG
MIR100HG
0.100 GeneticVariation disease GWASCAT A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1. 19779542 2009
Entrez Id: 4285
Gene Symbol: MIPEP
MIPEP
0.100 GeneticVariation disease GWASCAT Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population. 21640322 2011
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
Entrez Id: 105374266
Gene Symbol: LINC01991
LINC01991
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: 1501
Gene Symbol: CTNND2
CTNND2
0.010 GeneticVariation disease BEFREE Specific polymorphisms in the CTNND2 gene and 11q24.1 genomic region were found to be significantly associated with pathological myopia in this Chinese population, further supporting the idea that these genomic regions carry susceptibility loci for this disease. 22759899 2012