rs1057519047, FGFR2

N. diseases: 1
Disease: Pfeiffer Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pfeiffer Syndrome
CUI: C0220658
Disease: Pfeiffer Syndrome
0.800 GeneticVariation CLINVAR
Pfeiffer Syndrome
CUI: C0220658
Disease: Pfeiffer Syndrome
0.800 GeneticVariation UNIPROT