Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7938889
rs7938889
Entrez Id: 84441
Gene Symbol: MAML2
MAML2
CUI: C0017638
Disease:
Glioma
0.010 GeneticVariation BEFREE MAML2 rs7938889 and rs485842 polymorphisms were associated with the reduced risk of glioma (OR = 0.69, P=0.023; and OR = 0.81, P=0.032, respectively). 31652449 2019