rs16849225

Parent Gene: FIGN, GRB14

Importance: 2
Less common allele: T = 23%
More common allele: C = 77%
My Genotype: Log In
Risk Allele: C, T

Disease/Trait: Systolic Blood Pressure

The C allele of rs16849225 is reported to be associated with Systolic Blood Pressure (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Blood pressure (Systolic).

Disease/Trait: Systolic Blood Pressure

The T allele of rs16849225 is reported to be associated with Systolic Blood Pressure (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Systolic blood pressure (East Asians).