Disease: Oculovestibuloauditory syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852763
rs137852763
Entrez Id: 4361
Gene Symbol: MRE11
MRE11
CUI: C0271270
Disease:
Oculovestibuloauditory syndrome 		0.010 GeneticVariation BEFREE The previously reported missense mutation W210C in MRE11 gene was identified in two families with autosomal recessive ataxia and oculomotor apraxia. 21324166 2011