[PMID 21347284] Genome-Wide Association Studies of the PR Interval in African Americans

rs3922844

Parent Gene: SCN5A

Importance: 2
Less common allele: T = 36%
More common allele: C = 64%
My Genotype: Log In
Risk Allele: C, T, C, C

Disease/Trait: Pr Interval

The C allele of rs3922844 is reported to be associated with Pr Interval (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with PR interval.

Disease/Trait: Pr Interval

The T allele of rs3922844 is reported to be associated with Pr Interval (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with PR interval.

Disease/Trait: Qrs Duration

The C allele of rs3922844 is reported to be associated with Qrs Duration (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with QRS duration (African American).

Disease/Trait: Qrs Duration

The C allele of rs3922844 is reported to be associated with Qrs Duration (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with QRS duration (European).