Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs876657699
rs876657699
0.010 GeneticVariation BEFREE A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C>T (p.Arg259*) in the <i>MITF</i> gene in Yakut patient from the Eastern Siberia (Sakha Republic, Russia). 31213145

2019