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Obsessive-compulsive disorder (OCD) DNA health report

Follow the link of the selected polymorphism to read a brief description of how the selected polymorphism affects Obsessive-compulsive disorder (OCD) and see a list of existing studies.

SNP polymorphisms related to the topic Obsessive-compulsive disorder (OCD):

rs890Glutamate receptor gene (GRIN2B) associated with reduced glutamatergic concentration in the anterior cingulate gyrus in obsessive-compulsive disorder in children.
rs4680The study showed a 10% increase in total plasma homocysteine (tHcy)
rs6265Increased risk of ADHD or depression. Slightly faster decline in mental abilities in patients with Alzheimer's disease. The presence of this BDNF polymorphism is associated with differences in brain motor system functioning, altered short-term plasticity, and greater error in short-term motor learning.
rs6267
rs6277Associated with a 1.6-fold increased risk of schizophrenia.
rs6296
rs6305Serotonin transporter and serotonin receptor gene polymorphisms are associated with susceptibility to substance abuse.
rs6311Genetic factors specific to obsessive-compulsive disorder.
rs6313TPH-2 polymorphisms affect response to treatment with antidepressants and SSRIs.
rs6314The serotonin receptor gene HTR2A polymorphism is associated with bipolar affective disorder and autism spectrum disorder.
rs25531The serotonin transporter rs25531 polymorphism is associated with neuroticism, depression, OCD, ADHD and autism spectrum disorder.
rs25532Each C rs25532 allele accounts for increased serotonin transporter function and is pathogenetically associated with OCD.
rs270722-fold risk of severe alcohol withdrawal. Associated with more severe symptoms after alcohol withdrawal, such as seizures and white fever. Possible increased chance of ADHD.
rs140700A variant of the serotonin transporter gene (SLC6A4) is associated with suicidal behaviour in schizophrenic patients.
rs165631
rs167771The dopamine receptor-3 (DRD3) gene is associated with specific repetitive behaviours in autism spectrum disorders.
rs211107
rs220597
rs297941
rs301430
rs301443Association between the glutamate transporter gene SLC1A1 and early onset of obsessive-compulsive disorder.
rs460000
rs676643
rs737865
rs737866
rs769224
rs849876
rs1019385
rs1062613Fear reactivation and symptoms of combat-related PTSD: specificity and preliminary study of the effect of the 5-HT3A receptor gene.
rs1081003
rs1125394The DRD2 polymorphism modulates reward and emotion processing, dopamine neurotransmission, and openness to experience.
rs1176713Common variants of the HTR3 gene are associated with obsessive-compulsive disorder.
rs1232487
rs1568214
rs1799913Variants in the tryptophan hydroxylase gene involved in the development and treatment of opiate, heroin and cocaine addiction.
rs1805088
rs1805476The glutamate receptor gene GRIN2B associated with reduced glutamatergic concentration in the anterior cingulate cortex in obsessive-compulsive disorder in children.
rs1805502
rs1806202
rs1843809Breakage of the tryptophan hydroxylase 2 (TPH2) gene associated with attention deficit hyperactivity disorder.
rs1928040Polymorphisms of the gene encoding serotonin 2A receptor affect response to antidepressant treatment.
rs2039290
rs2066713A functional serotonin transporter gene polymorphism is associated with major depression, schizophrenia and ADHD.
rs2150195
rs2160734
rs2228622Association between the SLC1A1 gene and early onset of obsessive-compulsive disorder.
rs2268102
rs2283265Functional variants of the dopamine receptor gene are a potential factor in neuropsychiatric disorders.
rs2300252
rs2617605
rs2734838
rs3087879A haplotype containing quantitative trait loci of SLC1A1 gene expression is associated with obsessive-compulsive disorder.
rs3177118
rs3737193
rs3742278Serotonin receptor gene HTR2A polymorphism is associated with panic disorder features.
rs3773678
rs3776512
rs3780412Association of the glutamate transporter gene SLC1A1 with atypical obsessive-compulsive symptoms induced by neuroleptics.
rs3780413
rs3780415
rs4460839
rs4565946
rs4570625The TPH2 gene variant is associated with attention-deficit/hyperactivity disorder.
rs4648317Tendency to higher nicotine dependence, increased impulsivity and thrill-seeking.
rs4742007
rs4764011
rs5993883
rs7022772
rs7124442
rs7224199Association with major depression and response to antidepressants. The polymorphism is associated with selective serotonin and serotonin-norepinephrine reuptake inhibitor response in depressive disorder.
rs7297761
rs7298664
rs7848533
rs7997012Associations of the serotonin receptor gene HTR2A with bipolar disorder and major depressive disorder.
rs9316232
rs9325202Breakage of the tryptophan hydroxylase gene promotes dishonest behaviour.
rs9332316
rs9332377
rs9499708
rs9567737
rs9652236
rs9824856
rs10232398
rs10499905
rs10748189
rs10814991
rs10835210
rs10879346
rs10974584
rs10974587
rs11214606
rs11657536
rs12579598
rs12583882
rs16921385
rs16965628A genetic polymorphism of the serotonin transporter gene, SLC6A4 rs16965628, is associated with obsessive-compulsive disorder.
rs17110563The gene breakage is linked to bipolar affective disorder.
rs17834128
rs28363168
rs28371725
rs28914829A polymorphism in the serotonin transporter locus (SLC6A4) predisposes to autism and compulsive rigid behaviour.
rs35815285
rs56232120
rs61888800
rs116567227
rs1057519438
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