rs17807815

Parent Gene: ATXN3

Importance: 3
Less common allele: C = 6%
More common allele: T = 94%
My Genotype: Log In
Risk Allele:

Disease/Trait: Orofacial Clefting Syndrome

rs17807815 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.