Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3788266
rs3788266
0.020 GeneticVariation BEFREE Higher mean serum S100B levels were associated with the risk G allele of rs3788266 in BPAD cases (P = 0.0001), unaffected relatives of BPAD cases (P < 0.0001) and unrelated controls (P < 0.0001). 21714070

2011

dbSNP: rs3788266
rs3788266
0.020 GeneticVariation BEFREE S100B single nucleotide polymorphisms (SNPs) rs2839350 (P = 0.022) and rs3788266 (P = 0.031) were significantly associated with BPAD. 17525977

2007

dbSNP: rs6265
rs6265
0.020 GeneticVariation BEFREE Haplotype analysis of marker combination rs988748-(GT)n-rs6265 produced nominally significant associations for all investigated phenotypes (global p values: MDD p = .00006, BPAD p = .0057, schizophrenia p = .016). 16005437

2005

dbSNP: rs6265
rs6265
0.020 GeneticVariation BEFREE Association analysis of brain-derived neurotrophic factor (BDNF) gene Val66Met polymorphism in schizophrenia and bipolar affective disorder. 15543516

2004

dbSNP: rs1062613
rs1062613
0.010 GeneticVariation BEFREE Three single nucleotide polymorphisms (SNPs) in the HTR3A and HTR3B genes (rs1062613, rs1176744 and rs3831455) have been associated with bipolar affective disorder (BPAD) in pilot studies, and all of them are of functional relevance. 22832903

2012

dbSNP: rs1106854
rs1106854
0.010 GeneticVariation BEFREE A mutation in intron four, rs1106854, was associated with BPAD, although a regulatory role for rs1106854 is unclear. 24817687

2014

dbSNP: rs1176744
rs1176744
0.010 GeneticVariation BEFREE Three single nucleotide polymorphisms (SNPs) in the HTR3A and HTR3B genes (rs1062613, rs1176744 and rs3831455) have been associated with bipolar affective disorder (BPAD) in pilot studies, and all of them are of functional relevance. 22832903

2012

dbSNP: rs1267969615
rs1267969615
ACE
0.010 GeneticVariation BEFREE In contrast, when studying the AGT M235T polymorphism we found that the M allele was more frequently observed in BPAD patients than in controls (chi(2)=6.766, d.f.=1, P=0.009). 11027844

2000

dbSNP: rs1386482
rs1386482
0.010 GeneticVariation BEFREE SNPs rs1386482 and rs1386486, which are in very strong linkage disequilibrium, were associated with BPAD (P=0.006). 19352219

2009

dbSNP: rs1386483
rs1386483
0.010 GeneticVariation BEFREE The associated SNPs are in perfect linkage disequilibrium with SNPs previously associated with BPAD (rs4290270) and impulsivity (rs1386483), a core trait of BPAD. 19352219

2009

dbSNP: rs1386486
rs1386486
0.010 GeneticVariation BEFREE SNPs rs1386482 and rs1386486, which are in very strong linkage disequilibrium, were associated with BPAD (P=0.006). 19352219

2009

dbSNP: rs1469698992
rs1469698992
0.010 GeneticVariation BEFREE A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: no role in the genetic predisposition to bipolar affective disorder. 8493294

1993

dbSNP: rs147837176
rs147837176
0.010 GeneticVariation BEFREE It therefore remains possible that Glu602Gly may be a rare cause of bipolar affective disorder. 10889530

2000

dbSNP: rs166508
rs166508
0.010 GeneticVariation BEFREE One single SNP (rs166508) was associated with the BPAD phenotype (P = 0.0187). 23280964

2013

dbSNP: rs169068
rs169068
0.010 GeneticVariation BEFREE For the British population we found association to B</span>PAD with missense mutation Leu48Met (P = 0.003) and missense mutation Pro335Leu (P = 0.004). 12192619

2002

dbSNP: rs17110563
rs17110563
0.010 GeneticVariation BEFREE Examination of the functional effects of TPH2 Pro206Ser provided evidence for a reduced thermal stability and solubility of the mutated enzyme, suggesting reduced 5-HT production in the brain as a pathophysiological mechanism in BPAD. 17905754

2008

dbSNP: rs2076137
rs2076137
0.010 GeneticVariation BEFREE Association was observed for rs2235349 and rs2076137 with SCZ and ss16339163 with BPAD in case-control study. 15992519

2005

dbSNP: rs2235349
rs2235349
0.010 GeneticVariation BEFREE Association was observed for rs2235349 and rs2076137 with SCZ and ss16339163 with BPAD in case-control study. 15992519

2005

dbSNP: rs2251219
rs2251219
0.010 GeneticVariation BEFREE There is strong evidence of association of rs2251219 with BP. 22560537

2012

dbSNP: rs2812393
rs2812393
0.010 GeneticVariation BEFREE Two-locus analysis showed C-C (rs766288-rs2812393) as a risk combination in BPAD, and G-T (rs2812393-rs821616) as a protective combination in SCZ and combined cases of BPAD or SCZ. 22673686

2012

dbSNP: rs2839350
rs2839350
0.010 GeneticVariation BEFREE S100B single nucleotide polymorphisms (SNPs) rs2839350 (P = 0.022) and rs3788266 (P = 0.031) were significantly associated with BPAD. 17525977

2007

dbSNP: rs34608001
rs34608001
0.010 GeneticVariation BEFREE For the Danish population, association was suggested between silent SNP G573A and BPAD (P = 0.008). 12192619

2002

dbSNP: rs3771829
rs3771829
0.010 GeneticVariation BEFREE To further elucidate the role of TACR1 in affective disorders, rs3771829 was genotyped in a second BPAD sample of 593 subjects (UCL2), in 997 subjects with ADS, and a subsample of 143 individuals diagnosed with BPAD and comorbid alcohol dependence (BPALC). rs3771829 was associated with BPAD (UCL1 and UCL2 combined: P = 2.0 × 10(-3)), ADS (P = 2.0 × 10(-3)) and BPALC (P = 6.0 × 10(-4)) compared with controls screened for the absence of mental illness and alcohol dependence. 24817687

2014

dbSNP: rs3831455
rs3831455
0.010 GeneticVariation BEFREE Three single nucleotide polymorphisms (SNPs) in the HTR3A and HTR3B genes (rs1062613, rs1176744 and rs3831455) have been associated with bipolar affective disorder (BPAD) in pilot studies, and all of them are of functional relevance. 22832903

2012

dbSNP: rs4290270
rs4290270
0.010 GeneticVariation BEFREE The associated SNPs are in perfect linkage disequilibrium with SNPs previously associated with BPAD (rs4290270) and impulsivity (rs1386483), a core trait of BPAD. 19352219

2009