rs12044355
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12044355(A;A) |
| Make rs12044355(A;C) |
| Make rs12044355(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 231708601 |
| Gene | DISC1, TSNAX-DISC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12044355 |
| dbSNP (classic) | rs12044355 |
| ClinGen | rs12044355 |
| ebi | rs12044355 |
| HLI | rs12044355 |
| Exac | rs12044355 |
| Gnomad | rs12044355 |
| Varsome | rs12044355 |
| LitVar | rs12044355 |
| Map | rs12044355 |
| PheGenI | rs12044355 |
| Biobank | rs12044355 |
| 1000 genomes | rs12044355 |
| hgdp | rs12044355 |
| ensembl | rs12044355 |
| geneview | rs12044355 |
| scholar | rs12044355 |
| rs12044355 | |
| pharmgkb | rs12044355 |
| gwascentral | rs12044355 |
| openSNP | rs12044355 |
| 23andMe | rs12044355 |
| SNPshot | rs12044355 |
| SNPdbe | rs12044355 |
| MSV3d | rs12044355 |
| GWAS Ctlg | rs12044355 |
| GMAF | 0.3255 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19118814 ]
|
| Trait | Alzheimer's disease |
| Title | Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease |
| Risk Allele | |
| P-val | 0.000009 |
| Odds Ratio | NR NR |
[PMID 20574532] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.
