[PMID 20532249] Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.


rs2742234

Parent Gene: RET

Importance: 3
Less common allele: C = 31%
More common allele: T = 69%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Hirschsprung Disease

The T allele of rs2742234 is reported to be associated with Hirschsprung Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Hirschsprung disease.