rs3746319
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3746319(C;C) |
| Make rs3746319(C;T) |
| Make rs3746319(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 44108078 |
| Gene | LOC100379224, ZNF224 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3746319 |
| dbSNP (classic) | rs3746319 |
| ClinGen | rs3746319 |
| ebi | rs3746319 |
| HLI | rs3746319 |
| Exac | rs3746319 |
| Gnomad | rs3746319 |
| Varsome | rs3746319 |
| LitVar | rs3746319 |
| Map | rs3746319 |
| PheGenI | rs3746319 |
| Biobank | rs3746319 |
| 1000 genomes | rs3746319 |
| hgdp | rs3746319 |
| ensembl | rs3746319 |
| geneview | rs3746319 |
| scholar | rs3746319 |
| rs3746319 | |
| pharmgkb | rs3746319 |
| gwascentral | rs3746319 |
| openSNP | rs3746319 |
| 23andMe | rs3746319 |
| SNPshot | rs3746319 |
| SNPdbe | rs3746319 |
| MSV3d | rs3746319 |
| GWAS Ctlg | rs3746319 |
| GMAF | 0.3664 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20574532
] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.
[PMID 21480501] Replication study of genome-wide associated SNPs with late-onset Alzheimer's disease.
[PMID 27103528] Association of genetic risk factors with cognitive decline: the PATH through life project.
