Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56010818
rs56010818
CYP1B1
0.010 GeneticVariation BEFREE The R390H mutation was identified as a predominant CYP1B1 allele among the Chinese PCG patients in our study. 19247456

2009