Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1392844787
rs1392844787
ZNF569
CUI: C0020608
Disease: Hypodontia
Hypodontia 		0.010 GeneticVariation BEFREE Searches for mutations in these candidate genes detected a novel nonsense mutation (c.416G>A) in exon 1 of MSX1 from a family with oligodontia. 24329876

2014