Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57096
Gene Symbol: RPGRIP1
RPGRIP1 		0.300 Biomarker disease CTD_human Null RPGRIP1 alleles in patients with Leber congenital amaurosis. 11283794 2001
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A 		0.110 Biomarker disease BEFREE Vertical nystagmus occurs most frequently in SCA3 and SCA6. 18418678 2008
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A 		0.110 Biomarker disease HPO
Entrez Id: 4361
Gene Symbol: MRE11
MRE11 		0.100 Biomarker disease HPO
Entrez Id: 23556
Gene Symbol: PIGN
PIGN 		0.100 Biomarker disease HPO
Entrez Id: 146057
Gene Symbol: TTBK2
TTBK2 		0.100 Biomarker disease HPO
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.100 CausalMutation disease CLINVAR
Entrez Id: 5830
Gene Symbol: PEX5
PEX5 		0.100 Biomarker disease HPO
Entrez Id: 5189
Gene Symbol: PEX1
PEX1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 4287
Gene Symbol: ATXN3
ATXN3 		0.010 Biomarker disease BEFREE Vertical nystagmus occurs most frequently in SCA3 and SCA6. 18418678 2008