rs11610206
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common on affy axiom data |
| Make rs11610206(C;C) |
| Make rs11610206(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 47245743 |
| Gene | LOC105369746 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11610206 |
| dbSNP (classic) | rs11610206 |
| ClinGen | rs11610206 |
| ebi | rs11610206 |
| HLI | rs11610206 |
| Exac | rs11610206 |
| Gnomad | rs11610206 |
| Varsome | rs11610206 |
| LitVar | rs11610206 |
| Map | rs11610206 |
| PheGenI | rs11610206 |
| Biobank | rs11610206 |
| 1000 genomes | rs11610206 |
| hgdp | rs11610206 |
| ensembl | rs11610206 |
| geneview | rs11610206 |
| scholar | rs11610206 |
| rs11610206 | |
| pharmgkb | rs11610206 |
| gwascentral | rs11610206 |
| openSNP | rs11610206 |
| 23andMe | rs11610206 |
| SNPshot | rs11610206 |
| SNPdbe | rs11610206 |
| MSV3d | rs11610206 |
| GWAS Ctlg | rs11610206 |
| GMAF | 0.1065 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 3E-7 |
| Odds Ratio | NR NR |
[PMID 20883677] Genetic association of rs11610206 SNP on chromosome 12q13 with late-onset Alzheimer's disease in a Han Chinese population
[PMID 20574532] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.
