[PMID 18978678] Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.

rs7677751

Parent Gene: PDGFRA

Importance: 4
Less common allele: T = 24%
More common allele: C = 76%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Astigmatism

The T allele of rs7677751 is reported to be associated with Astigmatism (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Corneal astigmatism.