Disease: Severe myopia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6203
rs6203
Entrez Id: 3283
Gene Symbol: HSD3B1
HSD3B1
CUI: C0271183
Disease:
Severe myopia 		0.010 GeneticVariation BEFREE An MDR analysis corroborated the synergistic genotype association and demonstrated that synergistic interaction between rs6203 (HSD3B1), rs10046 (CYP19A1), and sex might confer susceptibility to high myopia (p=0.019). 21921981 2011