Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113488022
rs113488022
CUI: C1513734
Disease: Solid/Multicystic Ameloblastoma
Solid/Multicystic Ameloblastoma
0.010 GeneticVariation BEFREE Taken together, our findings demonstrate high frequency of activating BRAF V600E mutations in both UAM and AM of the mandible. 30216733

2019