Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs301430
rs301430
0.060 GeneticVariation BEFREE In the present study, we aimed to assess the association of SLC1A1 polymorphisms (rs301430, rs2228622 and rs3780413) with OCD and its clinical characteristics, as well as the importance of these SNPs in the response of OCD patients to SSRI pharmacotherapy. 30315580

2019

dbSNP: rs301430
rs301430
0.060 GeneticVariation BEFREE The C-T-G haplotype at rs301430-rs301434-rs3087879 of SLC1A1 was significantly associated with higher PD scores after adjusted for age, sex, and OCD status. 29304071

2018

dbSNP: rs301430
rs301430
0.060 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: rs301430
rs301430
0.060 GeneticVariation BEFREE Two haplotypes at 3 SNPs, rs3087879, rs301430, and rs7858819, were significantly associated with OCD after multiple-testing correction and contained 2 SNPs associated with expression levels. 19349310

2009

dbSNP: rs301430
rs301430
0.060 GeneticVariation BEFREE Additionally, an rs301430-rs301979 haplotype identified for OCD was investigated. 19360657

2008

dbSNP: rs301430
rs301430
0.060 GeneticVariation BEFREE Association between OCD and the three-marker haplotype rs12682807/ rs2072657/ rs301430, with overtransmission of A/T/T, was observed in both genders combined (global P = 0.0015) and in males (global P = 0.0031). 17894418

2007

dbSNP: rs301434
rs301434
0.040 GeneticVariation BEFREE The A-A-G (rs301434-rs3780412-rs301443) haplotype was twice as common in OCD as in controls (P = 0.02). 30661718

2019

dbSNP: rs301434
rs301434
0.040 GeneticVariation BEFREE The C-T-G haplotype at rs301430-rs301434-rs3087879 of SLC1A1 was significantly associated with higher PD scores after adjusted for age, sex, and OCD status. 29304071

2018

dbSNP: rs301434
rs301434
0.040 GeneticVariation BEFREE To test for association between SLC1A1 and autism, we typed three single nucleotide polymorphisms (SNPs, rs301430, rs301979, rs301434) previously associated with OCD in 86 strictly defined trios with autism. 19360657

2008

dbSNP: rs301434
rs301434
0.040 GeneticVariation BEFREE After correction for multiple comparisons, 2 variants, rs301434 (chi 2 = 12.04; P = .006) and rs301435 (chi 2 = 9.24; P = .03), located within a single haplotype block were found to be associated with transmission of OCD. 16818866

2006

dbSNP: rs2228622
rs2228622
0.030 GeneticVariation BEFREE In the present study, we aimed to assess the association of SLC1A1 polymorphisms (rs301430, rs2228622 and rs3780413) with OCD and its clinical characteristics, as well as the importance of these SNPs in the response of OCD patients to SSRI pharmacotherapy. 30315580

2019

dbSNP: rs2228622
rs2228622
0.030 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: rs2228622
rs2228622
0.030 GeneticVariation BEFREE Single-marker associations with OCD in the region (rs3780412 and rs2228622) demonstrated modest significance (permuted P = 0.045). 17894418

2007

dbSNP: rs3780412
rs3780412
0.020 GeneticVariation BEFREE The A-A-G (rs301434-rs3780412-rs301443) haplotype was twice as common in OCD as in controls (P = 0.02). 30661718

2019

dbSNP: rs3087879
rs3087879
0.020 GeneticVariation BEFREE The C-T-G haplotype at rs301430-rs301434-rs3087879 of SLC1A1 was significantly associated with higher PD scores after adjusted for age, sex, and OCD status. 29304071

2018

dbSNP: rs3087879
rs3087879
0.020 GeneticVariation BEFREE For the most strongly associated SNP (rs3087879), one copy of the risk allele increased the probability of higher treatment resistance (odds ratio=2.42; 95% confidence interval=1.39-4.21; P=0.0018), but only in OCD patients without life stress at onset of the disorder. 22776887

2013

dbSNP: rs3780412
rs3780412
0.020 GeneticVariation BEFREE Single-marker associations with OCD in the region (rs3780412 and rs2228622) demonstrated modest significance (permuted P = 0.045). 17894418

2007

dbSNP: rs3780413
rs3780413
0.010 GeneticVariation BEFREE In the present study, we aimed to assess the association of SLC1A1 polymorphisms (rs301430, rs2228622 and rs3780413) with OCD and its clinical characteristics, as well as the importance of these SNPs in the response of OCD patients to SSRI pharmacotherapy. 30315580

2019

dbSNP: rs12682807
rs12682807
0.010 GeneticVariation BEFREE Secondary analyses of male-affecteds only (N = 358 trios and 133 cases) demonstrated modest association between OCD and a different SNP (rs12682807; uncorrected P = 0.012; non-significant corrected P). 23606572

2013

dbSNP: rs7858819
rs7858819
0.010 GeneticVariation BEFREE Two haplotypes at 3 SNPs, rs3087879, rs301430, and rs7858819, were significantly associated with OCD after multiple-testing correction and contained 2 SNPs associated with expression levels. 19349310

2009

dbSNP: rs301979
rs301979
0.010 GeneticVariation BEFREE Additionally, an rs301430-rs301979 haplotype identified for OCD was investigated. 19360657

2008

dbSNP: rs301435
rs301435
0.010 GeneticVariation BEFREE After correction for multiple comparisons, 2 variants, rs301434 (chi 2 = 12.04; P = .006) and rs301435 (chi 2 = 9.24; P = .03), located within a single haplotype block were found to be associated with transmission of OCD. 16818866

2006