Disease: Primary congenital glaucoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893622
rs104893622
Entrez Id: 1545
Gene Symbol: CYP1B1
CYP1B1
CUI: C1533041
Disease:
Primary congenital glaucoma 		0.010 GeneticVariation BEFREE Eight distinct mutations were identified: G61E, R469W and D374N, the most common Saudi mutations, account for 72, 12 and 7%, respectively, of all the PCG chromosomes. 10655546 2000