Parent Gene: SH3BP4

Importance: 3
Less common allele: None = None
More common allele: None = None
My Genotype: Log In
Risk Allele:

Disease/Trait: Orofacial Clefting Syndrome

rs10174126 is associated with Orofacial Clefting Syndrome (R) . It is reported to increased association with Orofacial clefts (CP). No specific risk allele was identified in the study.