rs1051169
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1051169(C;C) |
| Make rs1051169(C;G) |
| Make rs1051169(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 46602317 |
| Gene | S100B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1051169 |
| dbSNP (classic) | rs1051169 |
| ClinGen | rs1051169 |
| ebi | rs1051169 |
| HLI | rs1051169 |
| Exac | rs1051169 |
| Gnomad | rs1051169 |
| Varsome | rs1051169 |
| LitVar | rs1051169 |
| Map | rs1051169 |
| PheGenI | rs1051169 |
| Biobank | rs1051169 |
| 1000 genomes | rs1051169 |
| hgdp | rs1051169 |
| ensembl | rs1051169 |
| geneview | rs1051169 |
| scholar | rs1051169 |
| rs1051169 | |
| pharmgkb | rs1051169 |
| gwascentral | rs1051169 |
| openSNP | rs1051169 |
| 23andMe | rs1051169 |
| SNPshot | rs1051169 |
| SNPdbe | rs1051169 |
| MSV3d | rs1051169 |
| GWAS Ctlg | rs1051169 |
| Merged from | Rs11542311 |
| GMAF | 0.4252 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
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| ||
[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 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 21070816] Risk variants in the S100B gene, associated with elevated S100B levels, are also associated with visuospatial disability of schizophrenia.
[PMID 29529989] S100B polymorphisms are associated with age of onset of Parkinson's disease.
