rs10121009
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10121009(C;C) |
| Make rs10121009(C;T) |
| Make rs10121009(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 35269822 |
| Gene | UNC13B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10121009 |
| dbSNP (classic) | rs10121009 |
| ClinGen | rs10121009 |
| ebi | rs10121009 |
| HLI | rs10121009 |
| Exac | rs10121009 |
| Gnomad | rs10121009 |
| Varsome | rs10121009 |
| LitVar | rs10121009 |
| Map | rs10121009 |
| PheGenI | rs10121009 |
| Biobank | rs10121009 |
| 1000 genomes | rs10121009 |
| hgdp | rs10121009 |
| ensembl | rs10121009 |
| geneview | rs10121009 |
| scholar | rs10121009 |
| rs10121009 | |
| pharmgkb | rs10121009 |
| gwascentral | rs10121009 |
| openSNP | rs10121009 |
| 23andMe | rs10121009 |
| SNPshot | rs10121009 |
| SNPdbe | rs10121009 |
| MSV3d | rs10121009 |
| GWAS Ctlg | rs10121009 |
| GMAF | 0.3485 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21812969 ]
|
| Trait | |
| Title | Genome-Wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. |
| Risk Allele | A |
| P-val | 0.000003 |
| Odds Ratio | None None |
[PMID 18633107] G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes.
