rs227731

Parent Gene: C17ORF67, NOG

Importance: 3
Less common allele: G = 48%
More common allele: T = 52%
My Genotype: Log In
Risk Allele: C, C, C

Disease/Trait: Progranulin Measurement

The C allele of rs227731 is reported to be associated with Progranulin Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Orofacial clefts (Meta-All, NSCL/P).

Disease/Trait: Cleft Lip

The C allele of rs227731 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.

Disease/Trait: Cleft Lip

rs227731 is associated with Cleft Lip (R) . It is reported to increased association with Cleft lip with or without cleft palate. No specific risk allele was identified in the study.

Disease/Trait: Cleft Palate

rs227731 is associated with Cleft Palate (R) . It is reported to increased association with Cleft lip with or without cleft palate. No specific risk allele was identified in the study.

Disease/Trait: Cleft Lip

The C allele of rs227731 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 Nonsyndromic cleft lip with cleft palate.

Disease/Trait: Cleft Palate

The C allele of rs227731 is reported to be associated with Cleft Palate (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Nonsyndromic cleft lip with cleft palate.