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.