Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
0.080 GeneticVariation BEFREE A fixed-effect model was chosen, and the pooled result showed that rs6296 was not related to al</span>coholism (z = 1.93, <i>p</i> = .053). 31510870 2019
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
0.080 GeneticVariation BEFREE The aim of this study is to investigate the role of the most relevant variants (rs11568817, rs130058, rs6296 and rs13212041) of the HTR1B gene in the susceptibility to alcohol dependence. 22005095 2012
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
0.080 GeneticVariation BEFREE Our study suggests that neither the 5-HTTLPR gene nor the 5-HT1B G861C polymorphism alone is a risk factor for antisocial alcoholism in Taiwan's Han Chinese population, but that the interaction between both genes may increase susceptibility to antisocial alcoholism. 22550993 2012
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
0.080 GeneticVariation BEFREE No significant association of the genotype or allele frequencies of the h5-HTR(1B) G861C locus was observed with diagnoses of alcoholism, bipolar disorder, schizophrenia or a history of a suicide attempt. 12496953 2003
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
0.080 GeneticVariation BEFREE There exists preliminary evidence for association of G861C with i) antisocial alcoholism in the Finnish; ii) alcoholism in the presence of inactive aldehyde dehydrogenase 2 in the Japanese; iii) a history of suicide attempts in European-American personality disorder patients; and iv) minimum lifetime body mass index in Canadian bulimia nervosa patients. 12437478 2002
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
0.080 GeneticVariation BEFREE Consequently, genes encoding serotonin (5-HT) receptors are candidates for genetic studies of both disorders. found evidence for linkage of antisocial alcoholism to HTR1B (the locus encoding the 5-HT1B receptor) in both Finns and Southwestern American Indians, and of allelic association of a G861C polymorphism at that locus with antisocial alcoholism in Finns. 11751038 2002
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
0.080 GeneticVariation BEFREE The HTR1B 861G>C receptor polymorphism among patients suffering from alcoholism, major depression, anxiety disorders and narcolepsy. 11104852 2000
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
0.080 GeneticVariation BEFREE In the Southwestern American Indian tribe, significant sib pair linkage of antisocial alcoholism</span> to HTR1B G861C (P=.01) was again observed, and there was also significant linkage to D6S284 (P=.01). 9819067 1998
Attention deficit hyperactivity disorder
0.050 GeneticVariation BEFREE The results showed that the 861G allele of 5-HTR1B SNP rs6296 could significantly increase the risk of ADHD (C)R=1.09, 95% CI: 1.01-1.18); the 5-HTR2C gene rs518147 (OR=1.69, 95% CI: 1.38-2.07) and rs3813929 (OR = 1.57, 95% CI: 1.25-1.97) were all associated with the risk of ADHD. 30074224 2018
Attention deficit hyperactivity disorder
0.050 GeneticVariation BEFREE Taking into account the well-known sexual dimorphic effect observed in serotonergic system characteristics, we differentially tested the influence of HTR1B SNPs (rs11568817, rs130058, rs6296 and rs13212041) on ADHD susceptibility and on its major comorbidities according to sex. 28923721 2017
Attention deficit hyperactivity disorder
0.050 GeneticVariation BEFREE We measured neural activation during stop-signal task performance in adolescents with ADHD (N = 185), their unaffected siblings (N = 111), and healthy controls (N = 124), and investigated the relationship of two serotonin gene polymorphisms (the rs6296 SNP of the HTR1B gene and HTTLPR variants of the 5-HTT gene) with the neural correlates of response inhibition. 26428549 2015
Attention deficit hyperactivity disorder
0.050 GeneticVariation BEFREE We used the transmission disequilibrium test (TDT) and haplotype analysis to investigate the A-161T and G861C polymorphisms in the 5-HT1B receptor gene in ADHD trios from the Chinese Han population. 15578608 2005
Attention deficit hyperactivity disorder
0.050 GeneticVariation BEFREE We tested for linkage disequilibrium between the 5-HT1B G861C polymorphism and ADHD in 115 families using the transmission disequilibrium test (TDT). 12556913 2003
Headache
CUI: C0018681
Disease: Headache
0.030 GeneticVariation BEFREE Gene polymorphisms including serotonin (5-HT)(1B) receptor G861C and dopamine receptor 2 (DRD2) C939T, personality traits and characteristics of headache were investigated in 46 consistent responders and 14 inconsistent responders to triptans. 21822697 2012
Antisocial behavior
CUI: C0233523
Disease: Antisocial behavior
0.030 GeneticVariation BEFREE Therefore, we examined whether the 5-HTTLPR gene and 5-HT1B gene G861C polymorphism are susceptibility factors for a specific subtype of alcoholism, antisocial alcoholism in Han Chinese in Taiwan. 22550993 2012
Headache
CUI: C0018681
Disease: Headache
0.030 GeneticVariation BEFREE Moreover, a positive association of the CC genotype of the G861C polymorphism of the 5-HT1B receptor with the reported intensity of the headache attack on the visual analogue scale was observed (CC 8.3 +/- 1.5 vs. GG 6.9 +/- 1.8; p < 0.05). 17417740 2007
Antisocial behavior
CUI: C0233523
Disease: Antisocial behavior
0.030 GeneticVariation BEFREE Consequently, genes encoding serotonin (5-HT) receptors are candidates for genetic studies of both disorders. found evidence for linkage of antisocial alcoholism to HTR1B (the locus encoding the 5-HT1B receptor) in both Finns and Southwestern American Indians, and of allelic association of a G861C polymorphism at that locus with antisocial alcoholism in Finns. 11751038 2002
Headache
CUI: C0018681
Disease: Headache
0.030 GeneticVariation BEFREE Allele frequencies of two polymorphisms in the 5-HT1B receptor gene (G861C and T-261G) were investigated in migraine patients with consistently good response to sumatriptan (n = 14), with no response (n = 12), with recurrence of the headache (n = 12), with chest symptoms (n = 13), and in patients without chest symptoms (n = 27). 9595868 1998
Antisocial behavior
CUI: C0233523
Disease: Antisocial behavior
0.030 GeneticVariation BEFREE In the Southwestern American Indian tribe, significant sib pair linkage of antisocial alcoholism to HTR1B G861C (P=.01) was again observed, and there was also significant linkage to D6S284 (P=.01). 9819067 1998
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
0.020 GeneticVariation BEFREE The rs6296-C allele lowered the level of HTR1B mRNA, causing individuals with MDD to display more hostility and aggressive behavior, which may lead to suicidal ideation. 28007644 2017
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
0.020 GeneticVariation BEFREE And the silent mutation G861C allele has been reported to be associated with several psychiatric disorders. 15698927 2005
Mental disorders
CUI: C0004936
Disease: Mental disorders
0.020 GeneticVariation BEFREE And the silent mutation G861C allele has been reported to be associated with several psychiatric disorders. 15698927 2005
Mental disorders
CUI: C0004936
Disease: Mental disorders
0.020 GeneticVariation BEFREE Interestingly, G861C has been reported to be associated with several psychiatric disorders. 14593427 2003
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
0.020 GeneticVariation BEFREE Substance abuse disorder and major depression are associated with the human 5-HT1B receptor gene (HTR1B) G861C polymorphism. 12496953 2003
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
0.020 GeneticVariation BEFREE Interestingly, G861C has been reported to be associated with several psychiatric disorders. 14593427 2003