Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137854438
rs137854438
0.010 GeneticVariation BEFREE Considering Fam83h<sup>-/-</sup> mice showed no enamel phenotype, while Fam83h<sup>Tr/Tr</sup> (p.Tyr297*) mice displayed obvious enamel malformations, we conclude that FAM83H truncation mutations causing ADHCAI in humans disturb amelogenesis through a neomorphic mechanism, rather than haploinsufficiency. 31060110

2019