rs12361953
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12361953(C;C) |
| Make rs12361953(C;G) |
| Make rs12361953(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 24589584 |
| Gene | LUZP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12361953 |
| dbSNP (classic) | rs12361953 |
| ClinGen | rs12361953 |
| ebi | rs12361953 |
| HLI | rs12361953 |
| Exac | rs12361953 |
| Gnomad | rs12361953 |
| Varsome | rs12361953 |
| LitVar | rs12361953 |
| Map | rs12361953 |
| PheGenI | rs12361953 |
| Biobank | rs12361953 |
| 1000 genomes | rs12361953 |
| hgdp | rs12361953 |
| ensembl | rs12361953 |
| geneview | rs12361953 |
| scholar | rs12361953 |
| rs12361953 | |
| pharmgkb | rs12361953 |
| gwascentral | rs12361953 |
| openSNP | rs12361953 |
| 23andMe | rs12361953 |
| SNPshot | rs12361953 |
| SNPdbe | rs12361953 |
| MSV3d | rs12361953 |
| GWAS Ctlg | rs12361953 |
| GMAF | 0.1189 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22881374 ]
|
| Trait | Alzheimer's disease (late onset) |
| Title | Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene. |
| Risk Allele | C |
| P-val | 8E-7 |
| Odds Ratio | NR NR |
Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene. (PMID:22881374 PMCID:PMC3419486), see TABLE 4 for reference to rs12361953 C allele.
