PRPH2, peripherin 2, 5961

N. diseases: 152; N. variants: 61
Disease: Retinitis Pigmentosa 7 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61755794
rs61755794
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2
CUI: C1842475
Disease:
Retinitis Pigmentosa 7 		A 0.800 CausalMutation CLINVAR
dbSNP: rs61755794
rs61755794
Entrez Id: 5961
Gene Symbol: PRPH2
PRPH2
CUI: C1842475
Disease:
Retinitis Pigmentosa 7 		0.800 GeneticVariation UNIPROT