Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23394
Gene Symbol: ADNP
ADNP 		0.100 Biomarker disease HPO
Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11 		0.100 CausalMutation disease CLINVAR
Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11 		0.100 Biomarker disease HPO
Entrez Id: 8943
Gene Symbol: AP3D1
AP3D1 		0.100 Biomarker disease HPO
Entrez Id: 51107
Gene Symbol: APH1A
APH1A 		0.010 Biomarker disease BEFREE Astigmatism has a significant influence on the higher-order aberrations, MTF, and PSF in the children. 28656103 2017
Entrez Id: 372
Gene Symbol: ARCN1
ARCN1 		0.100 Biomarker disease HPO
Entrez Id: 9181
Gene Symbol: ARHGEF2
ARHGEF2 		0.100 Biomarker disease HPO
Entrez Id: 57492
Gene Symbol: ARID1B
ARID1B 		0.100 Biomarker disease HPO
Entrez Id: 22901
Gene Symbol: ARSG
ARSG 		0.100 Biomarker disease HPO
Entrez Id: 417
Gene Symbol: ART1
ART1 		0.010 Biomarker disease BEFREE Comparison of visual quality in cataract patients with low astigmatism after ART2 or ReSTOR intraocular lens implantation. 30918811 2019
Entrez Id: 545
Gene Symbol: ATR
ATR 		0.010 Biomarker disease BEFREE Outcome comparisons between the two correction modalities were performed by grouping in different amounts (- 0.50 D, - 0.75 D) and axes (with the rule, WTR; against the rule, ATR; oblique, OBL) of astigmatism. 31641885 2020
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.100 Biomarker disease HPO
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 388552
Gene Symbol: BLOC1S3
BLOC1S3 		0.100 Biomarker disease HPO
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1 		0.100 Biomarker disease HPO
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.100 Biomarker disease HPO
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.100 Biomarker disease HPO
Entrez Id: 708
Gene Symbol: C1QBP
C1QBP 		0.100 Biomarker disease HPO
Entrez Id: 778
Gene Symbol: CACNA1F
CACNA1F 		0.110 Biomarker disease BEFREE Clinically, CORDX3 shares some features with CSNB2 but is distinguishable from CSNB2 in that it is progressive, can begin in adulthood, has no nystagmus or hyperopic refraction, has only low grade astigmatism, and in dark adaptation lacks cone threshold and has small or no elevation of rod threshold. 16505158 2006
Entrez Id: 778
Gene Symbol: CACNA1F
CACNA1F 		0.110 Biomarker disease HPO
Entrez Id: 401237
Gene Symbol: CASC15
CASC15 		0.110 GeneticVariation disease GWASCAT Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. 25367360 2015
Entrez Id: 401237
Gene Symbol: CASC15
CASC15 		0.110 Biomarker disease BEFREE Three of these loci also demonstrated genome-wide significant association with refractive astigmatism: LINC00340, HERC2/OCA2 and NPLOC4/TSPAN10. 30306274 2018
Entrez Id: 401237
Gene Symbol: CASC15
CASC15 		0.110 GeneticVariation disease GWASCAT Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. 30306274 2018
Entrez Id: 57545
Gene Symbol: CC2D2A
CC2D2A 		0.100 Biomarker disease HPO