Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs776587763
rs776587763
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0010278
Disease:
Craniosynostosis
0.710 GeneticVariation BEFREE C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients. 28849010 2017
dbSNP: rs776587763
rs776587763
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0010278
Disease:
Craniosynostosis
A 0.710 CausalMutation CLINVAR