Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909637
rs121909637
FGFR1
0.010 GeneticVariation BEFREE A mutation of TP63 (c.1010G>T; R337L) leads to SHFM with hypodontia. 31420900

2019