Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1564919048
rs1564919048
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0240310
Disease:
Hypoplasia of the maxilla
A 0.700 CausalMutation CLINVAR