Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918491
rs121918491
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C1867564
Disease:
SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY
T 0.700 CausalMutation CLINVAR