Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
0.070 GeneticVariation BEFREE Amongst neuropeptide S receptor gene functional sequence variants, the T-allele [asparagine(107)isoleucine, NPSR1 rs324981] has been identified as a risk factor for increased anxiety/overinterpretation of bodily symptoms. 27990720 2017
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
0.070 GeneticVariation BEFREE In recent years, accumulating data from various labs have demonstrated an A/T single-nucleotide polymorphism (SNP) resulting in (Asn107Ile) switch in the human NPSR gene as the risk factor for various psychiatric disorders such as panic disorder, post traumatic syndrome, alcohol use disorders and enhanced anxiety sensitivity, although, this is in stark contrast to the findings made in animal models which have consistently projected the anxiolytic nature of this peptide system. 26680586 2016
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
0.070 GeneticVariation BEFREE Thus, a gene-environment interaction (G × E) study of the neuropeptide S receptor gene (NPSR) A/T polymorphism (rs324981) and life events was conducted with respect to anxiety sensitivity (AS) as an intermediate phenotype of anxiety disorders. 22404660 2014
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
0.070 GeneticVariation BEFREE Since stress is critically involved in the pathogenesis of anxiety disorders, we tested the association between rs324981 and stress reactivity in 196 healthy males. 23466585 2013
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
0.070 GeneticVariation BEFREE The current results are in line with earlier imaging genetic studies and suggest a potential protective function of the NPSR1 rs324981 A/A genotype against pathologically enhanced anxiety that might be explained by stronger reflective prefrontal regulation over the subcortical fear response. 23103692 2013
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
0.070 GeneticVariation BEFREE All subjects were genotyped for the functional NPSR1 A/T (Asn(107)Ile) variant (rs324981) and characterized for anxiety sensitivity using the Anxiety Sensitivity Index (ASI). 23319044 2013
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
0.070 GeneticVariation BEFREE Thereby, NPSR rs324981 apparently causes an indirect effect on anxiety-related traits and potentially contributes to the pathogenesis of anxiety disorders by shaping fear-related limbic activity. 21525857 2011