Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10038177
rs10038177
0.010 GeneticVariation BEFREE First, a novel variation c.460-650A>G was found in our study which might cause premature termination of splicing of the conserved domain in <i>WDR36</i>; second, c.1494+1111G>T (rs13178997) had significantly different frequency in our JOAG patients compared to the reference frequency on NCBI; third, a variation c.710+30C>T (rs10038177) was found in our study, which had already been reported to be related to high-pressure glaucoma. 29104481

2017