rs769452
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs769452(C;C) |
| Make rs769452(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 44907853 |
| Gene | APOE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769452 |
| dbSNP (classic) | rs769452 |
| ClinGen | rs769452 |
| ebi | rs769452 |
| HLI | rs769452 |
| Exac | rs769452 |
| Gnomad | rs769452 |
| Varsome | rs769452 |
| LitVar | rs769452 |
| Map | rs769452 |
| PheGenI | rs769452 |
| Biobank | rs769452 |
| 1000 genomes | rs769452 |
| hgdp | rs769452 |
| ensembl | rs769452 |
| geneview | rs769452 |
| scholar | rs769452 |
| rs769452 | |
| pharmgkb | rs769452 |
| gwascentral | rs769452 |
| openSNP | rs769452 |
| 23andMe | rs769452 |
| SNPshot | rs769452 |
| SNPdbe | rs769452 |
| MSV3d | rs769452 |
| GWAS Ctlg | rs769452 |
| GMAF | 0.001377 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs769452(C;C) |
| Alt | rs769452(C;C) |
| Reference | Rs769452(T;T) |
| Significance | Pathogenic |
| Disease | APOE4(-)-FREIBURG not specified |
| Variation | info |
| Gene | APOE |
| CLNDBN | APOE4(-)-FREIBURG not specified |
| Reversed | 0 |
| HGVS | NC_000019.9:g.45411110T>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019456.28, RCV000429606.1, |
[PMID 17672902
] Subarachnoid hemorrhage: tests of association with apolipoprotein E and elastin genes.
