rs1292564852, FGFR3

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Agenesis
CUI: C0000846
Disease: Agenesis
0.010 GeneticVariation BEFREE Novel Wnt10A mutations (c.521T>C and c.653T>G) and EVC2 mutation (c.1472C>T) were identified in families with selective tooth agenesis. 30417976 2019