rs11872184

Parent Gene: SMCHD1

Importance: 3
Less common allele: A = 6%
More common allele: G = 94%
My Genotype: Log In
Risk Allele:

Disease/Trait: Conotruncal Heart Malformations

rs11872184 is associated with Conotruncal Heart Malformations (R) . It is reported to increased association with Conotruncal heart defects (EA, Inherited). No specific risk allele was identified in the study.