rs11983798
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common genotype |
| Make rs11983798(A;A) |
| Make rs11983798(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 105640741 |
| Gene | ATXN7L1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11983798 |
| dbSNP (classic) | rs11983798 |
| ClinGen | rs11983798 |
| ebi | rs11983798 |
| HLI | rs11983798 |
| Exac | rs11983798 |
| Gnomad | rs11983798 |
| Varsome | rs11983798 |
| LitVar | rs11983798 |
| Map | rs11983798 |
| PheGenI | rs11983798 |
| Biobank | rs11983798 |
| 1000 genomes | rs11983798 |
| hgdp | rs11983798 |
| ensembl | rs11983798 |
| geneview | rs11983798 |
| scholar | rs11983798 |
| rs11983798 | |
| pharmgkb | rs11983798 |
| gwascentral | rs11983798 |
| openSNP | rs11983798 |
| 23andMe | rs11983798 |
| SNPshot | rs11983798 |
| SNPdbe | rs11983798 |
| MSV3d | rs11983798 |
| GWAS Ctlg | rs11983798 |
| GMAF | 0.06107 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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 | T |
| P-val | 1E-6 |
| 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 rs11983798 T allele.
