rs10518765
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10518765(A;A) |
| Make rs10518765(A;C) |
| Make rs10518765(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 54388434 |
| Gene | UNC13C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10518765 |
| dbSNP (classic) | rs10518765 |
| ClinGen | rs10518765 |
| ebi | rs10518765 |
| HLI | rs10518765 |
| Exac | rs10518765 |
| Gnomad | rs10518765 |
| Varsome | rs10518765 |
| LitVar | rs10518765 |
| Map | rs10518765 |
| PheGenI | rs10518765 |
| Biobank | rs10518765 |
| 1000 genomes | rs10518765 |
| hgdp | rs10518765 |
| ensembl | rs10518765 |
| geneview | rs10518765 |
| scholar | rs10518765 |
| rs10518765 | |
| pharmgkb | rs10518765 |
| gwascentral | rs10518765 |
| openSNP | rs10518765 |
| 23andMe | rs10518765 |
| SNPshot | rs10518765 |
| SNPdbe | rs10518765 |
| MSV3d | rs10518765 |
| GWAS Ctlg | rs10518765 |
| GMAF | 0.1387 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 17903293 ]
|
| Trait | Select biomarker traits |
| Title | Genome-wide association with select biomarker traits in the Framingham Heart Study |
| Risk Allele | |
| P-val | 9.9999999999999995E-7 |
| Odds Ratio | NR NR |
[PMID 17052657] Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.
