Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs589249
rs589249
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
G 0.800 GeneticVariation GWASCAT A comprehensive family-based replication study of schizophrenia genes. 23894747

2013

dbSNP: rs589249
rs589249
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
G 0.800 GeneticVariation GWASDB A comprehensive family-based replication study of schizophrenia genes. 23894747

2013

dbSNP: rs10211550
rs10211550
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026

2017

dbSNP: rs10503899
rs10503899
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASDB Multifaceted genomic risk for brain function in schizophrenia. 22440650

2012

dbSNP: rs12773625
rs12773625
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203

2019

dbSNP: rs13295747
rs13295747
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASDB Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. 22037555

2011

dbSNP: rs145501595
rs145501595
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026

2017

dbSNP: rs16956732
rs16956732
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASDB Genome-wide association study identifies five new schizophrenia loci. 21926974

2011

dbSNP: rs4597906
rs4597906
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASDB Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. 24253340

2013

dbSNP: rs76432012
rs76432012
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
T 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764

2015

dbSNP: rs9656169
rs9656169
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASCAT Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study. 31268507

2019

dbSNP: rs9656169
rs9656169
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026

2017

dbSNP: rs9677260
rs9677260
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
T 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764

2015

dbSNP: rs1799732
rs1799732
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.050 GeneticVariation BEFREE The -141C Ins/Del polymorphism in DRD2 (rs1799732) is functional and associated with SCZ. 31176829

2019

dbSNP: rs1799732
rs1799732
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.050 GeneticVariation BEFREE A single nucleotide polymorphism, -141C insertion/deletion (Ins/Del) (rs1799732), in the promoter region of the dopamine D2 receptor gene has been linked to schizophrenia; however, the data are inconclusive. 26346037

2016

dbSNP: rs1799732
rs1799732
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.050 GeneticVariation BEFREE No significant associations were observed between rs1799732 and rs1800rs732 and rs1800497 and schizophrenia. 25504812

2015

dbSNP: rs1799732
rs1799732
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.050 GeneticVariation BEFREE Thus the aim of the present study was to investigate the possible association between the -141 Ins/Del (rs1799732) polymorphism of the dopamine receptor type 2 (DRD2) and schizophrenia. 19547807

2009

dbSNP: rs1799732
rs1799732
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.050 GeneticVariation BEFREE To test the hypothesis that DRD2 polymorphisms are associated with schizophrenia, we investigated two DRD2-related polymorphisms (TaqI A1/A2 or rs1800497 and -141-C Ins/Del or rs1799732) in a Spanish population isolate from northern Spain consisting of 165 controls and 119 patients with schizophrenia. 17417059

2007

dbSNP: rs1422636
rs1422636
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 GeneticVariation BEFREE The A-A-G-G-G-A-A rs9325104-rs1422636-rs7715569-rs6873382-rs7711800-rs10078551-rs2068190 haplotype was overrepresented in the schizophrenia cases. 19892407

2010

dbSNP: rs1700
rs1700
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 GeneticVariation BEFREE We found nominal association between brain-expressed miRNAs and schizophrenia for rs17578796 and rs1700 located in mir-206 and mir-198 respectively. 17849003

2007

dbSNP: rs1815774
rs1815774
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 GeneticVariation BEFREE Seven microsatellite or single-nucleotide polymorphism (SNP) markers localized within or near the FXYD6 gene showed empirically significant allelic associations with schizophrenia in the UCL sample (for D11S1998, P=.021; for rs3168238, P=.009; for TTTC20.2, P=.048; for rs1815774, P=.049; for rs4938445, P=.010; for rs4938446, P=.025; for rs497768, P=.023). 17357072

2007

dbSNP: rs3168238
rs3168238
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 GeneticVariation BEFREE Seven microsatellite or single-nucleotide polymorphism (SNP) markers localized within or near the FXYD6 gene showed empirically significant allelic associations with schizophrenia in the UCL sample (for D11S1998, P=.021; for rs3168238, P=.009; for TTTC20.2, P=.048; for rs1815774, P=.049; for rs4938445, P=.010; for rs4938446, P=.025; for rs497768, P=.023). 17357072

2007

dbSNP: rs363430
rs363430
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 GeneticVariation BEFREE We genotyped Japanese samples of schizophrenia (n = 193-203) and healthy controls (n = 199-215) for three SNPs those were commonly observed in our samples, 522A/C, 1173C/T, and 2705C/T. 11702055

2001

dbSNP: rs3747802
rs3747802
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 GeneticVariation BEFREE In this study, we investigated whether 9 SNPs in ABCB1 (rs6946119, rs28401781, rs4148739, and rs3747802), ABCB6 (rs1109866, rs1109867, rs3731885, and rs3755047), and ABCG1 (rs182694) contribute to the risk of SCZ in a Han Chinese population. 31189171

2019

dbSNP: rs490460
rs490460
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 GeneticVariation BEFREE Our data indicate that rs490460 is associated with the risk of SZ. 28384043

2017