Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs183532
rs183532
MYOC
0.020 GeneticVariation BEFREE Two SNPs rs183532 and rs235875 as well as a haplotype TTC in <i>MYOC</i> were nominally associated with PACG despite the significance was lost after Bonferroni correction. 31456923

2019
dbSNP: rs183532
rs183532
MYOC
0.020 GeneticVariation BEFREE Our study suggests that rs183532 is associated with an increased risk of PACG in the Chinese Han population. 25268471

2015