rs11708996

Parent Gene: SCN5A

Importance: 5
Less common allele: C = 9%
More common allele: G = 91%
My Genotype: Log In
Risk Allele: C, C, C, C

Disease/Trait: Heart Function Measurement

The C allele of rs11708996 is reported to be associated with Heart Function Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with QRS duration.

Disease/Trait: Pr Interval

The C allele of rs11708996 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: Qt Interval

The C allele of rs11708996 is reported to be associated with Qt Interval (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with QT interval.

Disease/Trait: Brugada Syndrome

The C allele of rs11708996 is reported to be associated with Brugada Syndrome (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Brugada syndrome.

Disease/Trait: Qrs Complex

rs11708996 is associated with Qrs Complex (R) . It is reported to association with QRS duration (EA). No specific risk allele was identified in the study.

Disease/Trait: Qrs Duration

rs11708996 is associated with Qrs Duration (R) . It is reported to association with QRS duration (EA). No specific risk allele was identified in the study.