Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs515726227
rs515726227
MSX1
CAT 0.710 CausalMutation CLINVAR In this study, we identified a novel heterozygous non-stop mutation (c.910_911dupTA, p.*304Tyrext*48) in MSX1 in a Chinese family with autosomal dominant non-syndromic oligodontia. 24914010

2014
dbSNP: rs515726227
rs515726227
MSX1
0.710 GeneticVariation BEFREE In this study, we identified a novel heterozygous non-stop mutation (c.910_911dupTA, p.*304Tyrext*48) in MSX1 in a Chinese family with autosomal dominant non-syndromic oligodontia. 24914010

2014
dbSNP: rs515726227
rs515726227
MSX1
CAT 0.710 CausalMutation CLINVAR A human MSX1 homeodomain missense mutation causes selective tooth agenesis. 8696335

1996