Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs936306
rs936306
Entrez Id: 1588;109729174
Gene Symbol: CYP19A1;MIR4713HG
CYP19A1;MIR4713HG
CUI: C0086132
Disease:
Depressive Symptoms
0.010 GeneticVariation BEFREE In Japanese women, the odds of depressive symptoms were nearly 5-fold higher among those with CYP 19 rs936306 TT genotype (95% CI, 1.10 to 22.17) than in women with the CC genotype and 9.6-fold higher (95% CI, 2.01 to 45.81) than in women with the CT genotype. 16949393 2006