rs10501927
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10501927(G;G) |
| Make rs10501927(G;T) |
| Make rs10501927(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 99886997 |
| Gene | CNTN5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10501927 |
| dbSNP (classic) | rs10501927 |
| ClinGen | rs10501927 |
| ebi | rs10501927 |
| HLI | rs10501927 |
| Exac | rs10501927 |
| Gnomad | rs10501927 |
| Varsome | rs10501927 |
| LitVar | rs10501927 |
| Map | rs10501927 |
| PheGenI | rs10501927 |
| Biobank | rs10501927 |
| 1000 genomes | rs10501927 |
| hgdp | rs10501927 |
| ensembl | rs10501927 |
| geneview | rs10501927 |
| scholar | rs10501927 |
| rs10501927 | |
| pharmgkb | rs10501927 |
| gwascentral | rs10501927 |
| openSNP | rs10501927 |
| 23andMe | rs10501927 |
| SNPshot | rs10501927 |
| SNPdbe | rs10501927 |
| MSV3d | rs10501927 |
| GWAS Ctlg | rs10501927 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20558387
] Genetic variation and neuroimaging measures in Alzheimer disease.
