rs7990916
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7990916(C;C) |
| Make rs7990916(C;T) |
| Make rs7990916(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 80065389 |
| Gene | LOC101927216 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7990916 |
| dbSNP (classic) | rs7990916 |
| ClinGen | rs7990916 |
| ebi | rs7990916 |
| HLI | rs7990916 |
| Exac | rs7990916 |
| Gnomad | rs7990916 |
| Varsome | rs7990916 |
| LitVar | rs7990916 |
| Map | rs7990916 |
| PheGenI | rs7990916 |
| Biobank | rs7990916 |
| 1000 genomes | rs7990916 |
| hgdp | rs7990916 |
| ensembl | rs7990916 |
| geneview | rs7990916 |
| scholar | rs7990916 |
| rs7990916 | |
| pharmgkb | rs7990916 |
| gwascentral | rs7990916 |
| openSNP | rs7990916 |
| 23andMe | rs7990916 |
| SNPshot | rs7990916 |
| SNPdbe | rs7990916 |
| MSV3d | rs7990916 |
| GWAS Ctlg | rs7990916 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25019275] Lack of association of a genetic variant in the long intergenic noncoding RNA (linc01080) with Alzheimer's disease and amnestic mild cognitive impairment in Han Chinese
