Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs759834365
rs759834365
0.010 GeneticVariation BEFREE Association analysis of brain-derived neurotrophic factor (BDNF) gene Val66Met polymorphism in schizophrenia and bipolar affective disorder. 15543516

2004

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: 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: rs4988483
rs4988483
0.010 GeneticVariation BEFREE For the British population we found association to BPAD with missense mutation Leu48Met</span> (P = 0.003) and missense mutation Pro335Leu (P = 0.004). 12192619

2002

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

2000

dbSNP: rs699
rs699
AGT
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: rs4680
rs4680
0.010 GeneticVariation BEFREE Because of its role in catecholamine metabolism and several lines of evidence pointing to a locus for psychosis near the COMT gene on chromosome 22q11, we have analysed the COMT Val158Met polymorphism as a candidate susceptibility factor for bipolar affective disorder. 9352569

1997

dbSNP: rs6318
rs6318
0.010 GeneticVariation BEFREE We have examined a structural variant of the 5-HT2C receptor (Cys23Ser) for allelic association with bipolar affective disorder in 88 cases and 113 controls. 8823764

1996

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: rs6280
rs6280
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