Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56149945
rs56149945
NR3C1
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency 		0.010 GeneticVariation BEFREE Potential advantage of N363S glucocorticoid receptor polymorphism in 21-hydroxylase deficiency. 16728546

2006