Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs746830376
rs746830376
EPHB2
CUI: C0521158
Disease: Recurrent tumor
Recurrent tumor 		0.010 GeneticVariation BEFREE However, we identified a co-occurring somatic HRAS (p.Q61R) activating point mutation and MEN1 frameshift mutation (p.L117fs) present in a primary and recurrent tumor from one patient. 27175596

2016