Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs929626
rs929626
0.710 GeneticVariation GWASCAT A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling. 28630421

2017

dbSNP: rs929626
rs929626
0.710 GeneticVariation BEFREE Analysis of phenotypic variability led to the identification of a specific genetic risk factor that approached genome-wide significance (rs929626 in EBF1 (Early B-Cell Factor 1); P = 2.04 × 10<sup>-7</sup>; OR = 0.7; 95% confidence interval (CI) = 0.61-0.8) with independent replication (P = 0.04), suggesting a variant-mediated dysregulation of leptin signaling may play a role in AN. 28630421

2017

dbSNP: rs11174202
rs11174202
0.700 GeneticVariation GWASCAT Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. 30087453

2018

dbSNP: rs12504244
rs12504244
0.700 GeneticVariation GWASCAT Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. 30087453

2018

dbSNP: rs75063949
rs75063949
0.700 GeneticVariation GWASCAT Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. 30087453

2018

dbSNP: rs6265
rs6265
0.080 GeneticVariation BEFREE Higher reward value of starvation imagery in anorexia nervosa and association with the Val66Met BDNF polymorphism. 27271855

2016

dbSNP: rs6265
rs6265
0.080 GeneticVariation BEFREE No difference was found in minimum BMIs related to Val66Met in AN (one-way ANOVA, P > 0.05). 22127997

2012

dbSNP: rs6265
rs6265
0.080 GeneticVariation BEFREE Our analyses indicate that the BDNF Val66Met variant is not associated with AN at detectable levels. 21936709

2013

dbSNP: rs6265
rs6265
0.080 GeneticVariation BEFREE BDNF has been involved in body weight regulation and its Val66Met polymorphism associated with AN. 17197106

2007

dbSNP: rs6265
rs6265
0.080 GeneticVariation BEFREE Some studies have shown association of BDNF -270C/T single-nucleotide polymorphism (SNP) with bulimia nervosa (BN), while BDNF Val66Met variant has been shown to be associated with both BN and anorexia nervosa (AN). 17376155

2007

dbSNP: rs6265
rs6265
0.080 GeneticVariation BEFREE Case-control studies also suggest a BDNF contribution in the aetiology of ED: we have previously reported a strong association between the Met66 variant within the BDNF gene, restricting AN (ANR) and minimum body mass index (minBMI) in a Spanish sample, and a positive association between the Val66Met and -270C/T BDNF SNPs and ED in six different European populations. 15657604

2005

dbSNP: rs6265
rs6265
0.080 GeneticVariation BEFREE We previously reported a strong association of the Met66 allele of the Val66Met BDNF variant with restricting AN (ANR) and low minimum body mass index in Spanish patients. 15115760

2004

dbSNP: rs6265
rs6265
0.080 GeneticVariation BEFREE Additionally, we genotyped two common polymorphisms (rs6265: p.V66M; c.-46C > T) in 118 patients with anorexia nervosa, 80 patients with bulimia nervosa, 88 patients with ADHD, and 96 normal weight controls. 15457498

2005

dbSNP: rs759834365
rs759834365
0.080 GeneticVariation BEFREE We previously reported a strong association of the Met66 allele of the Val66Met BDNF variant with restricting AN (ANR) and low minimum body mass index in Spanish patients. 15115760

2004

dbSNP: rs759834365
rs759834365
0.080 GeneticVariation BEFREE BDNF has been involved in body weight regulation and its Val66Met polymorphism associated with AN. 17197106

2007

dbSNP: rs759834365
rs759834365
0.080 GeneticVariation BEFREE Our analyses indicate that the BDNF Val66Met variant is not associated with AN at detectable levels. 21936709

2013

dbSNP: rs759834365
rs759834365
0.080 GeneticVariation BEFREE Higher reward value of starvation imagery in anorexia nervosa and association with the Val66Met BDNF polymorphism. 27271855

2016

dbSNP: rs759834365
rs759834365
0.080 GeneticVariation BEFREE Additionally, we genotyped two common polymorphisms (rs6265: p.V66M; c.-46C > T) in 118 patients with anorexia nervosa, 80 patients with bulimia nervosa, 88 patients with ADHD, and 96 normal weight controls. 15457498

2005

dbSNP: rs759834365
rs759834365
0.080 GeneticVariation BEFREE No difference was found in minimum BMIs related to Val66Met in AN (one-way ANOVA, P > 0.05). 22127997

2012

dbSNP: rs759834365
rs759834365
0.080 GeneticVariation BEFREE Some studies have shown association of BDNF -270C/T single-nucleotide polymorphism (SNP) with bulimia nervosa (BN), while BDNF Val66Met variant has been shown to be associated with both BN and anorexia nervosa (AN). 17376155

2007

dbSNP: rs759834365
rs759834365
0.080 GeneticVariation BEFREE Case-control studies also suggest a BDNF contribution in the aetiology of ED: we have previously reported a strong association between the Met66 variant within the BDNF gene, restricting AN (ANR) and minimum body mass index (minBMI) in a Spanish sample, and a positive association between the Val66Met and -270C/T BDNF SNPs and ED in six different European populations. 15657604

2005

dbSNP: rs4680
rs4680
0.060 GeneticVariation BEFREE The present study explores the effect of a functional polymorphism (Val158Met) in the catechol-O-methyltransferase (COMT) gene on the set-shifting abilities and prefrontal functional connectivity of patients with anorexia nervosa. 23046831

2013

dbSNP: rs4680
rs4680
0.060 GeneticVariation BEFREE Catechol-O-methyltransferase (COMT) is a candidate gene for mediating susceptibility to AN since it is involved in the dopamine catabolism and because its functional polymorphism (Val/Met 158) determines high (H) and low (L) enzymatic activity alleles. 11317231

2001

dbSNP: rs4680
rs4680
0.060 GeneticVariation BEFREE There were no significant group differences in COMT Val158Met alleles and genotype frequencies between patients and controls, for all EDs pooled together [range of odds ratios (ORs): 0.96-1.04, p-values: 0.46-0.97, I<sup>2</sup>  = 0%] and when analysing separately patients with AN (ORs: 0.94-1.04, p-values: 0.31-0.61, I<sup>2</sup>  = 0%) or BN (ORs: 0.80-1.09, p-values: 0.28-0.64, I<sup>2</sup>  = 0-44%). 29057600

2017

dbSNP: rs4680
rs4680
0.060 GeneticVariation BEFREE Association was found between AN-R and several SNPs in the COMT-ARVCF region including the 158Val/Met polymorphism. 16118784

2005