rs187980012, IGF1R

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fetal Growth Retardation
CUI: C0015934
Disease: Fetal Growth Retardation
0.010 GeneticVariation BEFREE We identified a family bearing a new heterozygous missense mutation at the L2 domain of IGF-IR (R431L) through an 8-year-old girl and her mother, both born with intrauterine growth retardation. 22309212 2012