Rs4938369
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs4938369 |
| hapmap | rs4938369 |
| hgdp | rs4938369 |
| ensembl | rs4938369 |
| gopubmed | rs4938369 |
| scholar | rs4938369 |
| rs4938369 | |
| pharmgkb | rs4938369 |
| hgvbaseg2p | rs4938369 |
| medrefsnp | rs4938369 |
| 23andMe | rs4938369 |
| SNP Nexus |
| Chromosome | 11 |
| Orientation | plus |
| Position | 116693329 |
| Genotype | Effect |
|---|---|
| rs4938369(C;C) | 1.6x increased risk for Alzheimer's |
| rs4938369(C;T) | ? |
| rs4938369(T;T) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs4938369(C;C) | 1.6x increased risk for Alzheimer's | |
| Rs4938369(C;T) | ? | |
| Rs4938369(T;T) | normal |
A case-control study (429 cases and 346 controls of Han Chinese descent) reported that rs4938369(C;C) homozygotes had a 1.67x higher risk for sporadic Alzheimer's disease than (C;T) or (T;T) individuals (odds ratio 1.667, CI: 1.087-2.556, p = 0.019).[PMID 19441127]
