[PMID 18612588] the C allele of rs2505535 would appear to represent a protecting allele for the Chinese population


[PMID 15759212] Identifying candidate Hirschsprung disease-associated RET variants.


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

rs2505535

Parent Gene: RET

Importance: 1
Less common allele: A = 25%
More common allele: G = 75%
My Genotype: Log In
Risk Allele: A

Disease/Trait: Blood Protein Measurement

The A allele of rs2505535 is reported to be associated with Blood Protein Measurement . Your genotype was not identified for this SNP so we are unable to comment on your association with Blood protein levels (Proto-oncogene tyrosine-protein kinase receptor Ret).