[PMID 23536526] Association and cumulative effects of GWAS-identified genetic variants for nonsyndromic orofacial clefts in a Chinese population

rs1873147

Parent Gene: IGKV2OR22-3, TPM1

Importance: 5
Less common allele: G = 50%
More common allele: A = 50%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Progranulin Measurement

The C allele of rs1873147 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).