Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913115
rs121913115
FGFR3
0.710 GeneticVariation BEFREE Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: prenatal diagnosis and literature review. 24411048

2013
dbSNP: rs121913115
rs121913115
FGFR3
G 0.710 CausalMutation CLINVAR