Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6297
rs6297
CUI: C0596887
Disease: mathematical ability
mathematical ability
T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018

dbSNP: rs6296
rs6296
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
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

dbSNP: rs6296
rs6296
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
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

dbSNP: rs6296
rs6296
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
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

dbSNP: rs6296
rs6296
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
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

dbSNP: rs6296
rs6296
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
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

dbSNP: rs6296
rs6296
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
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

dbSNP: rs6296
rs6296
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
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

dbSNP: rs6296
rs6296
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
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

dbSNP: rs6296
rs6296
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

dbSNP: rs6296
rs6296
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

dbSNP: rs6296
rs6296
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

dbSNP: rs6296
rs6296
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

dbSNP: rs6296
rs6296
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

dbSNP: rs6296
rs6296
CUI: C0018681
Disease: Headache
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

dbSNP: rs6296
rs6296
CUI: C0233523
Disease: Antisocial behavior
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

dbSNP: rs6296
rs6296
CUI: C0018681
Disease: Headache
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

dbSNP: rs6296
rs6296
CUI: C0233523
Disease: Antisocial behavior
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

dbSNP: rs6296
rs6296
CUI: C0018681
Disease: Headache
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

dbSNP: rs6296
rs6296
CUI: C0233523
Disease: Antisocial behavior
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

dbSNP: rs130058
rs130058
CUI: C0438696
Disease: Suicidal
Suicidal
0.020 GeneticVariation BEFREE The rs130058 SNP within the 5-HTR1B gene demonstrated a differential association with increasing suicidal ideation depending on antidepressant type. 21449676

2011

dbSNP: rs130058
rs130058
CUI: C0438696
Disease: Suicidal
Suicidal
0.020 GeneticVariation BEFREE A haplotype association study suggested that the rs11568817-rs130058 haplotype of the HTR1B gene is significantly associated with suicidal ideation in MD. 19897250

2009

dbSNP: rs6296
rs6296
CUI: C1269683
Disease: Major Depressive Disorder
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

dbSNP: rs6296
rs6296
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.020 GeneticVariation BEFREE And the silent mutation G861C allele has been reported to be associated with several psychiatric disorders. 15698927

2005

dbSNP: rs6296
rs6296
CUI: C0004936
Disease: Mental disorders
Mental disorders
0.020 GeneticVariation BEFREE And the silent mutation G861C allele has been reported to be associated with several psychiatric disorders. 15698927

2005