Disease: Severe myopia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs79204362
rs79204362
Entrez Id: 1545
Gene Symbol: CYP1B1
CYP1B1
CUI: C0271183
Disease:
Severe myopia 		0.010 GeneticVariation BEFREE Similarly, the probands with moderate to high myopia among those with p.E229K and p.R368H mutations was 20% (3 out of 16) in comparison to 18% (18 out of 104) of those who did not harbour these mutations (p = 0.59). 29168043 2018