Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315339
rs74315339
MYOC
0.030 GeneticVariation BEFREE MYOC mutations were found to account for 3% of POAG cases in our entire cohort (n=765) and Gln48His is the most common defect. 22736945

2012
dbSNP: rs74315339
rs74315339
MYOC
0.030 GeneticVariation BEFREE The MYOC Gln48His mutation is unique among Indian POAG patients. 22194650

2011
dbSNP: rs74315339
rs74315339
MYOC
0.030 GeneticVariation BEFREE The Gln48His mutation was detected in 9 different glaucoma patients (four POAG and five PCG). 15723004

2005