Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4354668
rs4354668
Entrez Id: 6506
Gene Symbol: SLC1A2
SLC1A2
CUI: C0036341
Disease:
Schizophrenia
0.040 GeneticVariation BEFREE <b>Conclusion:</b> The results of the present study did not indicate an association of polymorphism-181 A/C (rs4354668) in <i>SLC1A2</i> and rs2486001 in <i>SLC6A9</i> with onset of schizophrenia and its psychopathology in a Polish population. 31118638 2019
dbSNP: rs4354668
rs4354668
Entrez Id: 6506
Gene Symbol: SLC1A2
SLC1A2
CUI: C0036341
Disease:
Schizophrenia
0.040 GeneticVariation BEFREE We examined rs4354668 in 88 clinically stabilized patients with schizophrenia, treated with CRT and assessed at enrolment, at the end of CRT and after 3 months. 30539765 2018
dbSNP: rs4354668
rs4354668
Entrez Id: 6506
Gene Symbol: SLC1A2
SLC1A2
CUI: C0036341
Disease:
Schizophrenia
0.040 GeneticVariation BEFREE The rs4354668 SNP was identified to be significantly associated with SCZ in both datasets, and a similar pattern was also observed in the two-stage study on conducting imputation and haplotype association analyses. 26459047 2015
dbSNP: rs4354668
rs4354668
Entrez Id: 6506
Gene Symbol: SLC1A2
SLC1A2
CUI: C0036341
Disease:
Schizophrenia
0.040 GeneticVariation BEFREE To evaluate the effect of functional polymorphisms (rs4354668 and rs2731880) of the excitatory amino acid transporters (EAAT1 and 2) on the cognitive dysfunction that characterizes schizophrenia. 24956246 2014