Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1463326176
rs1463326176
CRYGD ; LOC100507443
0.010 GeneticVariation BEFREE We identified a missense P24T mutation in CRYGD that was responsible for coralliform cataract in our studied family. 24103489

2013
dbSNP: rs28931605
rs28931605
CRYGD ; LOC100507443
0.010 GeneticVariation BEFREE We identified a missense P24T mutation in CRYGD that was responsible for coralliform cataract in our studied family. 24103489

2013
dbSNP: rs150857132
rs150857132
CRYGD ; LOC100507443
0.010 GeneticVariation BEFREE This is the first reported case of a congenital coralliform cataract phenotype associated with the mutation of Gly61Cys (P.G61C) in the CRYGD gene; it demonstrates a possible mechanism of action for the mutant gene. 18334953

2008