rs80244589, GRB10

N. diseases: 1
Disease: Russell-Silver syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Russell-Silver syndrome
CUI: C0175693
Disease: Russell-Silver syndrome
0.010 GeneticVariation BEFREE A mutation analysis of GRB10 in 58 unrelated patients with RSS identified, within the N-terminal domain of the protein, a P95S substitution in two patients with RSS. 10856193 2000