rs7005606

Parent Gene: NRG1

Importance: 3
Less common allele: G = 35%
More common allele: T = 65%
My Genotype: Log In
Risk Allele: G

Disease/Trait: Hirschsprung Disease

rs7005606 is associated with Hirschsprung Disease (R) . It is reported to association with Hirschsprung disease. No specific risk allele was identified in the study.

Disease/Trait: Hirschsprung Disease

The G allele of rs7005606 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 (East Asian).