rs7914558

Parent Gene: CNNM2

Importance: 3
Less common allele: A = 44%
More common allele: G = 56%
My Genotype: Log In
Risk Allele: G

Disease/Trait: Schizophrenia

The G allele of rs7914558 is reported to be associated with Schizophrenia (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Schizophrenia.

Disease/Trait: Schizophrenia

rs7914558 is associated with Schizophrenia (R) . It is reported to association with Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) (Modelling analysis). No specific risk allele was identified in the study.

Disease/Trait: Bipolar Disorder

rs7914558 is associated with Bipolar Disorder (R) . It is reported to association with Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) (Modelling analysis). No specific risk allele was identified in the study.

Disease/Trait: Attention Deficit Hyperactivity Disorder

rs7914558 is associated with Attention Deficit Hyperactivity Disorder (R) . It is reported to association with Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) (Modelling analysis). No specific risk allele was identified in the study.

Disease/Trait: Unipolar Depression

rs7914558 is associated with Unipolar Depression (R) . It is reported to association with Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) (Modelling analysis). No specific risk allele was identified in the study.

Disease/Trait: Autism Spectrum Disorder

rs7914558 is associated with Autism Spectrum Disorder (R) . It is reported to association with Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) (Modelling analysis). No specific risk allele was identified in the study.