rs1805794, NBN

N. diseases: 41
Disease: Meningioma, benign, no ICD-O subtype ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Meningioma, benign, no ICD-O subtype
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
0.010 GeneticVariation BEFREE The NBN rs1805794 minor allele variant was associated with decreased meningioma risk (P(trend) .006). 20150366 2010