Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4401971
rs4401971
0.800 GeneticVariation GWASCAT Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. 24821223

2015

dbSNP: rs4401971
rs4401971
A 0.800 GeneticVariation GWASDB Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. 24821223

2015

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

2018

dbSNP: rs12536521
rs12536521
0.700 GeneticVariation GWASCAT Sex differences in the genetic architecture of obsessive-compulsive disorder. 30456828

2019

dbSNP: rs12635725
rs12635725
0.700 GeneticVariation GWASCAT Sex differences in the genetic architecture of obsessive-compulsive disorder. 30456828

2019

dbSNP: rs28696717
rs28696717
0.700 GeneticVariation GWASCAT Sex differences in the genetic architecture of obsessive-compulsive disorder. 30456828

2019

dbSNP: rs4785741
rs4785741
T 0.700 GeneticVariation GWASCAT Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD. 28641744

2017

dbSNP: rs6109227
rs6109227
0.700 GeneticVariation GWASDB Genome-wide association study of obsessive-compulsive disorder. 22889921

2013

dbSNP: rs6131293
rs6131293
0.700 GeneticVariation GWASDB Genome-wide association study of obsessive-compulsive disorder. 22889921

2013

dbSNP: rs6131295
rs6131295
0.700 GeneticVariation GWASDB Genome-wide association study of obsessive-compulsive disorder. 22889921

2013

dbSNP: rs10491734
rs10491734
0.020 GeneticVariation BEFREE The present study provided suggestive evidence that the rs10491734 was significantly associated with early-onset OCD in the Han Chinese population. 23564280

2013

dbSNP: rs10491734
rs10491734
0.020 GeneticVariation BEFREE This case-control study enrolled 578 obsessive-compulsive disorder (OCD) patients and 649 controls and genotyped rs10491734, rs2228622, rs301430 and rs301443 to replicate association of the SLC1A1 gene with OCD in ethnic Han Chinese. 23411042

2013

dbSNP: rs1000592
rs1000592
0.010 GeneticVariation BEFREE The case-control analyses revealed a nominal significant association of the HTR3D variant rs1000592 (p.H52R) with OCD (p=0.029) which was also evident after combination of the case-control and the trio-results (p=0.024). 23928294

2014

dbSNP: rs10042486
rs10042486
0.010 GeneticVariation BEFREE We concluded that among the HTR1A polymorphisms, only the association of rs10042486 CT genotype and OCD was statistically significant. 30232922

2019

dbSNP: rs10070190
rs10070190
0.010 GeneticVariation BEFREE Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD. 23337130

2013

dbSNP: rs11783752
rs11783752
0.010 GeneticVariation BEFREE Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD. 23337130

2013

dbSNP: rs17162912
rs17162912
0.010 GeneticVariation BEFREE We attempt to replicate the GWAS finding by investigating the association of the DISP1 rs17162912 polymorphism with SRI response in our sample of 112 European Caucasian OCD patients. 29953682

2018

dbSNP: rs2097063
rs2097063
0.010 GeneticVariation BEFREE When the OCD group and controls were compared, no significant difference was found between COMT -287A/G (rs2097063), 5-HTTLPR I/D polymorphisms, and OCD. 25751280

2015

dbSNP: rs2834070
rs2834070
0.010 GeneticVariation BEFREE Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD. 23337130

2013

dbSNP: rs3933331
rs3933331
0.010 GeneticVariation BEFREE In addition, another SNP correlating with SLC1A1 gene expression, rs3933331, was associated with an OCD-hoarding subphenotype as assessed by 2 independent, validated scales. 19349310

2009

dbSNP: rs4387163
rs4387163
0.010 GeneticVariation BEFREE Three SNPs are most strongly associated with OCD: rs11854486 (P = 0.00005 [0.046 after adjustment for multiple tests]; genetic relative risk (GRR) = 11.1 homozygous and 1.6 heterozygous) and rs4625687 [P = 0.00007 (after adjustment = 0.06); GRR = 2.4] on 15q; and rs4387163 (P = 0.0002 (after adjustment = 0.08); GRR = 1.97) on 1q. 22095678

2012

dbSNP: rs4740788
rs4740788
0.010 GeneticVariation BEFREE We also found that SNP rs4740788, located about 8.8 kb upstream of the gene, was associated with OCD in all families (P = 0.003) and in families with male affecteds (P = 0.002). 21445956

2011

dbSNP: rs2364841
rs2364841
0.700 GeneticVariation GWASCAT Sex differences in the genetic architecture of obsessive-compulsive disorder. 30456828

2019

dbSNP: rs165599
rs165599
0.010 GeneticVariation BEFREE A haplotype composed of three SNPs [rs2097603; rs4680 (158Val/Met); rs165599] representing the major linkage disequilibrium blocks in COMT and previously implicated in functional variation, was found to be associated with ADHD and OCD in 22q11.2DS individuals. 17949513

2008

dbSNP: rs2071592
rs2071592
0.010 GeneticVariation BEFREE Given the importance of NFKBIL1 in the immunological response, the present study investigated the -62A/T polymorphism (rs2071592), located in the promoter region of its gene (NFKBIL1), as a genetic risk factor for the development of obsessive-compulsive disorder. 19578685

2009