CCND1, cyclin D1, 595

N. diseases: 859; N. variants: 12
Disease: Meningioma, benign, no ICD-O subtype ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs603965
rs603965
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C1762616
Disease:
Meningioma, benign, no ICD-O subtype 		0.010 GeneticVariation BEFREE Moreover, in stratified analyses by type of disease, we noticed that the rs603965 polymorphism was significantly associated with the susceptibility to glioma, but such positive results were not detected in pituitary adenoma or meningioma. 30972946 2019