Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs301443
rs301443
SPATA6L
0.050 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: rs301443
rs301443
SPATA6L
0.050 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: rs301443
rs301443
SPATA6L
0.050 GeneticVariation BEFREE This revealed weak association between OCD and one of nine tested SLC1A1 polymorphisms (rs301443; uncorrected P = 0.046; non-significant corrected P). 23606572

2013
dbSNP: rs301443
rs301443
SPATA6L
0.050 GeneticVariation BEFREE We genotyped an additional 111 SNPs in or near SLC1A1, covering from 9 kb upstream to 84 kb downstream of the gene at average spacing of 1.7 kb per SNP, and conducted family-based association analyses in 1,576 participants in 377 families.We found that none of the surrounding markers were in linkage disequilibrium with rs301443, nor were any associated with OCD. 21445956

2011
dbSNP: rs301443
rs301443
SPATA6L
0.050 GeneticVariation BEFREE Interestingly, the strongest association in OCD has been found at rs301443 (P=0.000067) residing between SLC1A1 and JMJD2C at 9p24. 20410850

2010