rs1258763 Parent Gene: FMN1, GREM1 Importance: 3 Less common allele: T = 46% More common allele: C = 54% My Genotype: Log In Risk Allele: A Disease/Trait: Progranulin Measurement rs1258763 is associated with Progranulin Measurement (R) . It is reported to association with Orofacial clefts (Meta-All, NSCL/P). No specific risk allele was identified in the study. Disease/Trait: Cleft Lip The A allele of rs1258763 is reported to be associated with Cleft Lip (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Orofacial clefts.