Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84627
Gene Symbol: ZNF469
ZNF469 		0.110 GeneticVariation disease BEFREE ZNF469 missense mutation is involved in a syndrome with very thin cornea (brittle cornea syndrome). 22814818 2012
Entrez Id: 84627
Gene Symbol: ZNF469
ZNF469 		0.110 Biomarker disease HPO
Entrez Id: 91851
Gene Symbol: CHRDL1
CHRDL1 		0.100 Biomarker disease HPO
Entrez Id: 4166
Gene Symbol: CHST6
CHST6 		0.100 Biomarker disease HPO
Entrez Id: 11081
Gene Symbol: KERA
KERA 		0.100 Biomarker disease HPO
Entrez Id: 653509
Gene Symbol: SFTPA1
SFTPA1 		0.010 Biomarker disease BEFREE Our study found that corneal thinning and biomechanical decreasing synchronize with one another throughout the progression of the keratoconus, and SP-A1 could be a potential biomarker evaluating disease progression. 31263429 2019
Entrez Id: 1289
Gene Symbol: COL5A1
COL5A1 		0.010 GeneticVariation disease BEFREE Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus. 23513063 2013