rs6913660
From SNPedia
| Schizophrenia-associated SNP in major histocompatibility complex |
| Orientation | plus |
| Stabilized | plus |
| Make rs6913660(A;A) |
| Make rs6913660(A;C) |
| Make rs6913660(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 27123646 |
| Gene | HIST1H2BJ |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6913660 |
| dbSNP (classic) | rs6913660 |
| ClinGen | rs6913660 |
| ebi | rs6913660 |
| HLI | rs6913660 |
| Exac | rs6913660 |
| Gnomad | rs6913660 |
| Varsome | rs6913660 |
| LitVar | rs6913660 |
| Map | rs6913660 |
| PheGenI | rs6913660 |
| Biobank | rs6913660 |
| 1000 genomes | rs6913660 |
| hgdp | rs6913660 |
| ensembl | rs6913660 |
| geneview | rs6913660 |
| scholar | rs6913660 |
| rs6913660 | |
| pharmgkb | rs6913660 |
| gwascentral | rs6913660 |
| openSNP | rs6913660 |
| 23andMe | rs6913660 |
| SNPshot | rs6913660 |
| SNPdbe | rs6913660 |
| MSV3d | rs6913660 |
| GWAS Ctlg | rs6913660 |
| GMAF | 0.1047 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 19571809
] Common variants on chromosome 6p22.1 are associated with schizophrenia.
[PMID 19911060] Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint.
[PMID 22005930] Genome-wide association study of Alzheimer's disease with psychotic symptoms.
