rs7996217
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs7996217(G;G) |
| Make rs7996217(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 101348594 |
| Gene | NALCN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7996217 |
| dbSNP (classic) | rs7996217 |
| ClinGen | rs7996217 |
| ebi | rs7996217 |
| HLI | rs7996217 |
| Exac | rs7996217 |
| Gnomad | rs7996217 |
| Varsome | rs7996217 |
| LitVar | rs7996217 |
| Map | rs7996217 |
| PheGenI | rs7996217 |
| Biobank | rs7996217 |
| 1000 genomes | rs7996217 |
| hgdp | rs7996217 |
| ensembl | rs7996217 |
| geneview | rs7996217 |
| scholar | rs7996217 |
| rs7996217 | |
| pharmgkb | rs7996217 |
| gwascentral | rs7996217 |
| openSNP | rs7996217 |
| 23andMe | rs7996217 |
| SNPshot | rs7996217 |
| SNPdbe | rs7996217 |
| MSV3d | rs7996217 |
| GWAS Ctlg | rs7996217 |
| GMAF | 0.01148 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22628157 ]
|
| Trait | |
| Title | Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults. |
| Risk Allele | T |
| P-val | 7E-7 |
| Odds Ratio | None None |
