rs11139399
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11139399(C;C) |
| Make rs11139399(C;T) |
| Make rs11139399(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 81757826 |
| Gene | LOC101927502 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11139399 |
| dbSNP (classic) | rs11139399 |
| ClinGen | rs11139399 |
| ebi | rs11139399 |
| HLI | rs11139399 |
| Exac | rs11139399 |
| Gnomad | rs11139399 |
| Varsome | rs11139399 |
| LitVar | rs11139399 |
| Map | rs11139399 |
| PheGenI | rs11139399 |
| Biobank | rs11139399 |
| 1000 genomes | rs11139399 |
| hgdp | rs11139399 |
| ensembl | rs11139399 |
| geneview | rs11139399 |
| scholar | rs11139399 |
| rs11139399 | |
| pharmgkb | rs11139399 |
| gwascentral | rs11139399 |
| openSNP | rs11139399 |
| 23andMe | rs11139399 |
| SNPshot | rs11139399 |
| SNPdbe | rs11139399 |
| MSV3d | rs11139399 |
| GWAS Ctlg | rs11139399 |
| GMAF | 0.489 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22745009 ]
|
| Trait | |
| Title | Multiple loci influencing hippocampal degeneration identified by genome scan. |
| Risk Allele | C |
| P-val | 0.000001 |
| Odds Ratio | None None |
