Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE A single nucleotide polymorphism (SNP), rs1344706, in the Zinc Finger Protein 804A (ZNF804A) gene, has been implicated in susceptibility to schizophrenia by several genome-wide association studies, follow-up association studies and meta-analyses. 21457757

2011

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE We verified that ZNF804A was significantly related to psychiatric diseases, and the association between ZNF804A rs1344706 and psychosis (schizophrenia and bipolar disorder) did not vary with disease or ethnicity. 25667193

2015

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE ZNF804A SNP rs1344706 confers genome-wide risk for schizophrenia and bipolar disorder. 23562677

2013

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE No differences in ZNF804A-immunoreactive neurons were seen in schizophrenia or related to rs1344706 (P > .05). 25162540

2014

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE The biological function of ZNF804A rs1344706, the first genome-wide supported risk variant of schizophrenia, remains largely unknown. 28078547

2018

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE Put in perspective, ZNF804A rs1344706, not only had a significant main effect, but its SZ-specific effects were two orders of magnitude more widespread than that of CACNA1C rs1006737. 27790829

2017

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE Single-marker analysis revealed significant associations between 2 recently identified candidate schizophrenia susceptibility variants (rs1344706 and rs7597593) and a refined positive schizotypy phenotype characterized primarily by self-rated paranoia/ideas of reference. 23155182

2013

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE In this 2-stage study, we tested for an association between ZNF804A rs1344706 and cognitive functions known to be impaired in schizophrenia (IQ, episodic memory, working memory, and attention) in an Irish discovery sample. 20603450

2010

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE A recent candidate gene study, which replicated the positive association with rs1344706, identified another positive SNP (rs7597593) in ZNF804A associated with schizophrenia. 21349497

2011

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE Our result suggests that genetic variant rs1344706 might be associated with the development of schizophrenia in Asians. 28883732

2017

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE We conclude that rs1344706 or a yet unknown polymorphism in linkage disequilibrium is also involved in conferring susceptibility to schizophrenia in samples with different (Asian) ancestral backgrounds. 23590871

2013

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE The homozygous ZNF804A rs1344706 genotype (AA) conferred a high risk of sc</span>hizophrenia, and also exhibited significantly decreased resting functional coupling between the left hippocampus and right DLPFC (F(2,165) = 13.43, P < 0.001). 29611035

2018

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE rs1344706 risk allele carriers of schizophrenia had increased gray matter in the brain regions including frontal lobe, temporal lobe, and other brain regions, but the carriers of healthy individuals had decreased gray matter and white matter integrity in the frontal lobe, central network, and other brain regions. 30962687

2019

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE The common variant rs1344706 within the zinc-finger protein gene ZNF804A has been strongly implicated in schizophrenia (SZ) susceptibility by a series of recent genetic association studies. 24424391

2014

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE Though the two SNPs did not remain significant if we applied multiple corrections, our analysis should be interpreted as a primary replication study with in prior hypothesis, and rs1344706 and rs1366842 might confer a small but detectable risk of schizophrenia (and bipolar disorder) in Asians. 26866941

2016

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE We tested the effect of rs1344706 genotype in 89 schizophrenia patients on 3 basic cognitive domains (working memory, processing speed and attention) shown to be severely impaired in schizophrenia. 22948380

2012

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE In conclusion, the ZNF804A rs1344706 variant was not associated with schizophrenia in the Romanian population from Cluj Napoca (χ(2)=0.734, p=0.693). 22775511

2012

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE The current meta-analysis showed an association between rs1344706 and schizophrenia in Caucasian populations (P=0.028, OR=1.138, 95% CI: 1.014-1.278; P=0.004 for heterogeneity) and Asian populations (P=0.008, OR=1.092, 95% CI: 1.023-1.165; P=0.001 for heterogeneity), but not in other populations (P=0.286, OR=1.209, 95% CI: 0.853-1.714, P=0.120 for heterogeneity). 25526981

2014

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE Our results did not support the association of rs1344706 with schizophrenia in Han Chinese, and further association studies with large samples from other ethnic backgrounds and focus on more SNPs of ZNF804A are warranted. 26934312

2016

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE Taken together, the disconnectivity of the lHF-PCC tract seems to be a plausible intermediate phenotype that links rs1344706 and schizophrenia. 26654932

2016

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE Patients homozygous for the ZNF804A risk allele for schizophrenia (rs1344706 AA) showed poorer improvement of positive symptoms (7.35 ± 0.46) compared to patients with a protective allele (9.41 ± 0.71, P = 0.022). 21892778

2012

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE Using this method, we were able to replicate an association between ZNF804A rs1344706 variant and schizophrenia in a Turkish population. 21988329

2012

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE The association of rs1344706 with WM changes in schizophrenia patients and healthy controls was analyzed using a full-factorial 2×2 analysis of variance. 21911029

2012

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE CACNA1C-rs1006737 and ZNF804A-rs1344706 polymorphisms are among the most robustly associated with schizophrenia (SCZ) and bipolar disorder (BD), and recently with brain phenotypes. 30079586

2019

dbSNP: rs1344706
rs1344706
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 GeneticVariation BEFREE Although this data does not preclude the possibility of other functional variants in ZNF804A, it provides evidence that the rs1344706 SZ risk allele is the cis-regulatory variant directly responsible for this allelic expression imbalance in adult cortex. 24315717

2014