rs74315330, MYOCOS;MYOC

N. diseases: 9
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hydrophthalmos
CUI: C0020302
Disease: Hydrophthalmos
0.010 GeneticVariation BEFREE The presence of a P370L mutation of MYOC in all six glaucoma patients suggests a casual association between this mutation and juvenile glaucoma with goniodysgenesis. 19668597 2009