GNB3, G protein subunit beta 3, 2784

N. diseases: 192; N. variants: 10
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4310758
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H 		0.400 GeneticVariation disease UNIPROT Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness. 27063057 2016
CUI: C4310758
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H 		0.400 CausalMutation disease CLINVAR