rs1806201
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs1806201(A;A) |
| Make rs1806201(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 13564574 |
| Gene | GRIN2B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1806201 |
| dbSNP (classic) | rs1806201 |
| ClinGen | rs1806201 |
| ebi | rs1806201 |
| HLI | rs1806201 |
| Exac | rs1806201 |
| Gnomad | rs1806201 |
| Varsome | rs1806201 |
| LitVar | rs1806201 |
| Map | rs1806201 |
| PheGenI | rs1806201 |
| Biobank | rs1806201 |
| 1000 genomes | rs1806201 |
| hgdp | rs1806201 |
| ensembl | rs1806201 |
| geneview | rs1806201 |
| scholar | rs1806201 |
| rs1806201 | |
| pharmgkb | rs1806201 |
| gwascentral | rs1806201 |
| openSNP | rs1806201 |
| 23andMe | rs1806201 |
| SNPshot | rs1806201 |
| SNPdbe | rs1806201 |
| MSV3d | rs1806201 |
| GWAS Ctlg | rs1806201 |
| GMAF | 0.3072 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 16911840] Association study of polymorphisms in N-methyl-D-aspartate receptor 2B subunits (GRIN2B) gene with Korean alcoholism
[PMID 15812607] Polymorphisms in the NMDA subunit 2B are not associated with alcohol dependence and alcohol withdrawal-induced seizures and delirium tremens.
[PMID 18303265] Association analysis of GRIN2B, encoding N-methyl-D-aspartate receptor 2B subunit, and Alzheimer's disease.
[PMID 20882066
] Association between NMDA receptor subunit 2b gene polymorphism and Alzheimer's disease in Chinese Han population in Shanghai.
[PMID 21749895] Variations in the GRIN2B gene are associated with risky decision-making.
[PMID 21827795] Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization.
| ClinVar | |
|---|---|
| Risk | rs1806201(A;A) |
| Alt | rs1806201(A;A) |
| Reference | Rs1806201(G;G) |
| Significance | Probable-non-pathogenic |
| Disease | not provided not specified Intellectual Disability |
| Variation | info |
| Gene | GRIN2B |
| CLNDBN | not provided not specified Intellectual Disability, Dominant |
| Reversed | 0 |
| HGVS | NC_000012.11:g.13717508G>A |
| CLNSRC | ClinVar University of Chicago |
| CLNACC | RCV000084728.1, RCV000117194.2, RCV000377659.1, |
[PMID 24114429] A study of N-methyl-D-aspartate receptor gene (GRIN2B) variants as predictors of treatment-resistant major depression
[PMID 22484476] N-methyl-D-aspartate receptor 2B subunit (GRIN2B) gene variation is associated with alerting, but not with orienting and conflicting in the Attention Network Test.
[PMID 22850629] Glutamatergic GRIN2B and polyaminergic ODC1 genes in suicide attempts: associations and gene-environment interactions with childhood/adolescent physical assault.
[PMID 23408766] Assessment of NMDA receptor genes (GRIN2A, GRIN2B and GRIN2C) as candidate genes in the development of degenerative lumbar scoliosis.
[PMID 23644918] Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset.
[PMID 25660313] Meta-analysis of six genes (BDNF, DRD1, DRD3, DRD4, GRIN2B and MAOA) involved in neuroplasticity and the risk for alcohol dependence
[PMID 27325396] Dopamine D3 receptor Ser9Gly variant is associated with impulse control disorders in Parkinson's disease patients.
