Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2 		0.600 GeneticVariation disease UNIPROT In Vivo Analysis of Disease-Associated Point Mutations Unveils Profound Differences in mRNA Splicing of Peripherin-2 in Rod and Cone Photoreceptors. 26796962 2016
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2 		0.600 GeneticVariation disease UNIPROT A novel mutation in the RDS gene in an Italian family with pattern dystrophy. 16024869 2005
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2 		0.600 GeneticVariation disease UNIPROT Founder effect, seen in the British population, of the 172 peripherin/RDS mutation-and further refinement of genetic positioning of the peripherin/RDS gene. 9443872 1998
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2 		0.600 GeneticVariation disease UNIPROT Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene. 8485574 1993
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2 		0.600 GeneticVariation disease CLINVAR
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2 		0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2 		0.600 CausalMutation disease CLINVAR