rs4471226

Parent Gene: PAPPA2, RFWD2

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

Disease/Trait: Nitric Oxide Exhalation Measurement

The C allele of rs4471226 is reported to be associated with Nitric Oxide Exhalation Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Fractional exhaled nitric oxide (childhood).