Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		0.700 GeneticVariation disease UNIPROT Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus. 21976959 2011
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		0.700 GeneticVariation disease UNIPROT Mutational screening of VSX1 in keratoconus patients from the European population. 19763142 2010
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		0.700 GeneticVariation disease UNIPROT A novel VSX1 mutation identified in an individual with keratoconus in India. 19956409 2009
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		0.700 GeneticVariation disease UNIPROT Three VSX1 gene mutations, L159M, R166W, and H244R, are not associated with keratoconus. 18216574 2008
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		0.700 GeneticVariation disease UNIPROT VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation. 15623752 2005
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		0.700 Biomarker disease GENOMICS_ENGLAND VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells. 15051220 2004
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		0.700 GeneticVariation disease UNIPROT VSX1: a gene for posterior polymorphous dystrophy and keratoconus. 11978762 2002
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		0.700 CausalMutation disease CLINVAR
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		0.700 Biomarker disease CTD_human
Entrez Id: 84627
Gene Symbol: ZNF469
ZNF469 		0.100 CausalMutation disease CLINVAR
Entrez Id: 84627
Gene Symbol: ZNF469
ZNF469 		0.100 GeneticVariation disease CLINVAR