CHROMOSOME 16 GRIN2A 16p13.2 GENE VIEW GRIN2A · 16p13.2 16p14 16p12 rs11866328 — ~70,000 base pairs in the gene — ~14,000 uncommon variants · <1% of humans have them — ~1,000 common variants · >1% carry the alternate allele ALLELE STATE rs11866328 G / A · GRIN2A · 16p13.2 HOMOZYGOUS WILD TYPE (DOMINANT) 5′ 3′ G 5′ 3′ G HETEROZYGOUS 5′ 3′ G 5′ 3′ A HOMOZYGOUS ALTERNATE (RECESSIVE) 5′ 3′ A 5′ 3′ A G Guanine — reference allele A Adenine — variant allele genetics.jdge.cc

rs11866328

Gene: GRIN2A — Glutamate Ionotropic Receptor NMDA Type Subunit 2A Chr 16:9768699 16p13.2 Intron Variant
NCBI ↗ GeneCards ↗ Open Targets ↗ gnomAD ↗ OMIM ↗ ClinVar ↗ Varsome ↗ LOVD ↗

Population Frequencies12

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Total G 0.595048T 0.404952GG 0.356876GT/TG 0.476344TT 0.166781pop=477,214
African G 0.60631T 0.39369GG 0.36835GT/TG 0.475921TT 0.155729pop=42,818
African American G 0.60607T 0.39393GG 0.367924GT/TG 0.476299TT 0.155777pop=41,264
African Others G 0.6126T 0.3874GG 0.379665GT/TG 0.465894TT 0.15444pop=1,554
Asian G 0.81602T 0.18398GG 0.66601GT/TG 0.30003TT 0.03396pop=13,192
East Asian G 0.81849T 0.18151GG 0.669994GT/TG 0.296986TT 0.03302pop=10,418
European G 0.579534T 0.420466GG 0.336522GT/TG 0.486024TT 0.177453pop=384,236
Latin American 1 G 0.6054T 0.3946GG 0.369658GT/TG 0.47151TT 0.158832pop=5,616
Latin American 2 G 0.7022T 0.2978GG 0.493921GT/TG 0.416564TT 0.089515pop=11,350
Other G 0.64051T 0.35949GG 0.411093GT/TG 0.458829TT 0.130077pop=16,298
Other Asian G 0.8068T 0.1932GG 0.651045GT/TG 0.311464TT 0.037491pop=2,774
South Asian G 0.743T 0.257GG 0.556695GT/TG 0.37257TT 0.070734pop=3,704

Studies41

Unread Studies41
1
Dopamine receptor inhibition underlies both the therapeutic and adverse effects of antipsychotics, but the mechanisms modulating these effects in patients with schizophrenia remain …
2
The polymorphisms of IFNL3 associated with the outcomes of primary HBV infection remains controversial, the susceptibility has not been investigated across cohorts. So two cohorts, …
3
Gene-environment interactions increase psychosis risk (Gayer-Anderson et al. Soc Psychiatry Psychiatr Epidemiol 2020; 55(5):645-657). However, identifying the genetic …
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Gene-environment interactions increase the risk of psychosis. The objective of this study was to investigate gene-gene and gene-environment interactions in psychosis, …
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Gene-environment interactions increase the risk of psychosis. The objective of this study was to investigate gene-gene and gene-environment interactions in psychosis, …
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The vulnerability-stress-inflammation model is a well-known psychopathological model in patients with psychosis. It implies an imbalance of the microglia activation (M1/M2 …
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The dopamine, serotonin and glutamate systems are jointly involved in the pathogenesis and pharmacotherapy of schizophrenia. We formulated a hypothesis that polymorphic variants …
8
Liver cirrhosis (LC) and hepatocellular carcinoma (HCC) are progressions affected by genetic predispositions, and persistent hepatitis B virus infection also demonstrates …
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Цель. Сравнить Частоты Генотипов Полиморфных Вариантов Генов Grin2a И Grin2b В Группах Больных Шизофренией С Аддиктивным Поведением (Злоупотребление …
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Clinical Applications of Immunogenetics: Immunogenetics: A Molecular and Clinical Overview, Volume II provides readers with an exclusive, updated overview of scientific knowledge, …
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Tardive dyskinesia (TD) is an extrapyramidal side effect of the long-term use of antipsychotics. In the present study, the role of glutamatergic system genes in the …
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This study aimed to explore the relationship between CCNE1 gene single nucleotide polymorphisms (SNP rs1406 and rs3218038) and the incidence of hepatitis B virus-related …
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Genome-wide association studies have been performed to identify common genetic variants associated with hepatitis B (HB). However, little is known about copy number variations (…
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The ASCC3 subunit of the activating signal co-integrator complex is a dual-cassette Ski2-like nucleic acid helicase that provides single-stranded DNA for alkylation damage repair by …
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The management of chronic hepatitis B virus (CHB) infection is an area of massive unmet clinical need worldwide. In spite of the development of powerful nucleoside/nucleotide …
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Chronic hepatitis B (CHB) is a precursor to liver cirrhosis and hepatocellular carcinoma, caused by a Hepatitis B viral infection. Genome-wide association studies (GWASs) have been …
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… In addition, rs11866328 at GRIN2A has been reported to be associated with the disease progression of chronic HBV infection (18). In this study, the at-risk allele of rs11866328 was …
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… Genotype-phenotype association analyses performed on 10 SNPs along with the discrete attributes revealed rs11866328 (C>A) and rs12325652 (A>G) to be positively correlated with …
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Chronic hepatitis B (CHB) is the most common chronic liver disease resulting from viral infection and has become a serious threat to human health. Each year, about 1.2 million people …
20
An established theory for the pathogenesis of tardive dyskinesia is disturbed dopaminergic receptor sensitivity and/or dopaminergic intracellular signaling. We examined …
21
Infectious diseases are among the leading causes of human morbidity and mortality, with the greatest burden felt in the pediatric population. For any infectious disease, only a fraction of …
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More than a million childhood diarrhoeal episodes occur worldwide each year, and in developed countries a considerable part of them are caused by viral infections. In this study, we …
23
We have previously identified 8 SNPs in Han Chinese HBV carriers that are associated with disease progression. Although not well studied, genetic factors may also play a significant …
24
Belgium has seen major changes in its tax-benefit system over the past twenty years. These changes have, to a large extent, co-determined the evolution of disposable incomes of …
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… The variant rs11866328 (G/T), located in the glutamate receptor ionotropic N-methyl D-aspartate 2A (GRIN2A) gene, showed a significant association with disease progression (Table 1)…
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Recent genome-wide association studies (GWAS) have identified several common susceptibility loci associated with the risk of hepatocellular carcinoma (HCC) or chronic hepatitis B …
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Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) regulates T-cell activation and Th1/Th2 cytokine production and is involved in the immune response against Hepatitis B virus (…
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… A genome-wide association study with DNA pooling identifies the variant rs11866328 in the GRIN2A gene that affects disease progression of chronic HBV infection.Viral Immunol2011;…
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Advances in genomics are contributing to the development of more effective, personalized approaches to the prevention and treatment of infectious diseases. Genetic sequencing …
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… 16p GRIN2A rs11866328 Chinese 1944 progressed carriers/854 asymptomatic carriers … A genome-wide association study with DNA pooling identifies the variant rs11866328 in the …
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Vaccines are the most cost effective public health measure for preventing viral infection and limiting epidemic spread within susceptible populations. However, the efficacy of current …
32
Delayed encephalopathy after acute carbon monoxide poisoning (DEACMP) is more characteristic of anoxic encephalopathy than of other types of anoxia. Those who have the same …
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The glutamate receptor, N-methyl D-aspartate 2A (GRIN2A) gene that encodes the 2A subunit of the N-methyl D-aspartate (NMDA) receptor was recently shown to be involved in the …
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… Hum Mol Genet 20 ; 3884―3892 : 2011 24)Liu L, Li J, Yao J, et al : A genome-wide association study with DNA pooling identifies the variant rs11866328 in the GRIN2A gene that …
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Four types of antipsychotic-induced movement disorders: tardive dyskinesia (TD), parkinsonism, akathisia and tardive dystonia, subtypes of TD (orofacial and limb truncal …
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Host genetics play a vital role in determining clinical outcomes of hepatitis B virus (HBV) infection. To identify novel susceptibility loci to HBV progression, we carried out a genome-wide …
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… We revealed the important role of SNP rs11866328 on the gene … rs11866328 may affect an individual's susceptibility to HBV progression. Our research indicates that SNP rs11866328 …
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A genome-wide association study with DNA pooling identifies the variant study with DNA pooling identifies the variant rs11866328 in the GRIN2A gene that affects disease …
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A doença de Chagas é causada pelo protozoário Trypanosoma cruzi e atinge cerca de 12 milhões de pessoas no continente americano, a forma clássica de transmissão ocorre por …
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KAWAMATA, CEM Identification of possible genes related to Trypanosoma cruzi infection in the human host. 2011. 125 p.(Ph. D. Thesis Biology of the interactions between Hosts and …
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Genetic polymorphism of IFNAR-1 plays a large role in determining the clearance or chronicity after hepatitis B virus (HBV) exposure. However, it is not clear whether type I interferon …
Curated Studies0

These studies were determined to be useful for this variant — check "Unused Studies" further down if curious what didn't make the cut.

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Unused Studies0

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