rs9722
| Orientation | minus |
| Stabilized | minus |
| Make rs9722(C;C) |
| Make rs9722(C;T) |
| Make rs9722(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 46599326 |
| Gene | S100B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9722 |
| dbSNP (classic) | rs9722 |
| ClinGen | rs9722 |
| ebi | rs9722 |
| HLI | rs9722 |
| Exac | rs9722 |
| Gnomad | rs9722 |
| Varsome | rs9722 |
| LitVar | rs9722 |
| Map | rs9722 |
| PheGenI | rs9722 |
| Biobank | rs9722 |
| 1000 genomes | rs9722 |
| hgdp | rs9722 |
| ensembl | rs9722 |
| geneview | rs9722 |
| scholar | rs9722 |
| rs9722 | |
| pharmgkb | rs9722 |
| gwascentral | rs9722 |
| openSNP | rs9722 |
| 23andMe | rs9722 |
| SNPshot | rs9722 |
| SNPdbe | rs9722 |
| MSV3d | rs9722 |
| GWAS Ctlg | rs9722 |
| GMAF | 0.2557 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19497163] Association study of astrocyte-derived protein S100B gene polymorphisms with major depressive disorder in Chinese people.
[PMID 21070816] Risk variants in the S100B gene, associated with elevated S100B levels, are also associated with visuospatial disability of schizophrenia.
[PMID 22019077] S100B gene polymorphisms predict prefrontal spatial function in both schizophrenia patients and healthy individuals.
[PMID 15670788] SNPs and haplotypes in the S100B gene reveal association with schizophrenia.
[PMID 18939940] No association of the rs9722 C >T in the S100B gene and susceptibility to major depression in a Chinese population.
[PMID 19330775] Risk variants in the S100B gene predict elevated S100B serum concentrations in healthy individuals.
[PMID 20559426
] Serum S100B: a potential biomarker for suicidality in adolescents?
[PMID 29529989] S100B polymorphisms are associated with age of onset of Parkinson's disease.
[PMID 32590820] Association of S100B 3'UTR polymorphism with risk of chronic heart failure in a Chinese Han population.
