rs16879552

Parent Gene: NRG1

Importance: 3
Less common allele: T = 21%
More common allele: C = 79%
My Genotype: Log In
Risk Allele: G

Disease/Trait: Hirschsprung Disease

The G allele of rs16879552 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.