Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs752829138
rs752829138
MYOC ; MYOCOS
0.010 GeneticVariation BEFREE In the MYOC gene, two variants of unknown significance (p.L228S and p.E240G) were identified in two PCG patients (2/85; 2.4%), respectively.No patient had mutations in both genes. 21850185

2011