rs10089
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10089(C;C) |
| Make rs10089(C;T) |
| Make rs10089(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 128186851 |
| Gene | SLC12A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10089 |
| dbSNP (classic) | rs10089 |
| ClinGen | rs10089 |
| ebi | rs10089 |
| HLI | rs10089 |
| Exac | rs10089 |
| Gnomad | rs10089 |
| Varsome | rs10089 |
| LitVar | rs10089 |
| Map | rs10089 |
| PheGenI | rs10089 |
| Biobank | rs10089 |
| 1000 genomes | rs10089 |
| hgdp | rs10089 |
| ensembl | rs10089 |
| geneview | rs10089 |
| scholar | rs10089 |
| rs10089 | |
| pharmgkb | rs10089 |
| gwascentral | rs10089 |
| openSNP | rs10089 |
| 23andMe | rs10089 |
| SNPshot | rs10089 |
| SNPdbe | rs10089 |
| MSV3d | rs10089 |
| GWAS Ctlg | rs10089 |
| GMAF | 0.2461 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21139019 ]
|
| Trait | |
| Title | A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | 2.5600 [1.79-3.70] |
[PMID 18520591] Sequence variants in host cell factor C1 are associated with Meniere's disease.
