rs10503929
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 |
| Make rs10503929(C;C) |
| Make rs10503929(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 32756465 |
| Gene | NRG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10503929 |
| dbSNP (classic) | rs10503929 |
| ClinGen | rs10503929 |
| ebi | rs10503929 |
| HLI | rs10503929 |
| Exac | rs10503929 |
| Gnomad | rs10503929 |
| Varsome | rs10503929 |
| LitVar | rs10503929 |
| Map | rs10503929 |
| PheGenI | rs10503929 |
| Biobank | rs10503929 |
| 1000 genomes | rs10503929 |
| hgdp | rs10503929 |
| ensembl | rs10503929 |
| geneview | rs10503929 |
| scholar | rs10503929 |
| rs10503929 | |
| pharmgkb | rs10503929 |
| gwascentral | rs10503929 |
| openSNP | rs10503929 |
| 23andMe | rs10503929 |
| SNPshot | rs10503929 |
| SNPdbe | rs10503929 |
| MSV3d | rs10503929 |
| GWAS Ctlg | rs10503929 |
| GMAF | 0.09183 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19435634] Three-cohort targeted gene screening reveals a non-synonymous TRKA polymorphism associated with schizophrenia
[PMID 22183611
] Genetic associations between neuregulin-1 SNPs and neurocognitive function in multigenerational, multiplex schizophrenia families
[PMID 22574178] Comprehensive Analysis of NRG1 Common and Rare Variants in Hirschsprung Patients
[PMID 17631867] Evidence of missense mutations on the neuregulin 1 gene affecting function of prepulse inhibition.
[PMID 18478032] Neuregulin 1 in neural development, synaptic plasticity and schizophrenia.
[PMID 20921115] Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls.
[PMID 21035784] The influence of schizophrenia-related neuregulin-1 polymorphisms on sensorimotor gating in healthy males.
[PMID 23524320] A Common Missense Variant in the Neuregulin1 Gene is associated with Both Schizophrenia and Sudden Cardiac Death
[PMID 24622944] Striatal Response to Reward Anticipation: Evidence for a Systems-Level Intermediate Phenotype for Schizophrenia
[PMID 29326614] Prediction Analysis for Transition to Schizophrenia in Individuals at Clinical High Risk for Psychosis: The Relationship of DAO, DAOA, and NRG1 Variants with Negative Symptoms and Cognitive Deficits.
