rs769455
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs769455(C;T) |
| Make rs769455(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 44908783 |
| Gene | APOE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769455 |
| dbSNP (classic) | rs769455 |
| ClinGen | rs769455 |
| ebi | rs769455 |
| HLI | rs769455 |
| Exac | rs769455 |
| Gnomad | rs769455 |
| Varsome | rs769455 |
| LitVar | rs769455 |
| Map | rs769455 |
| PheGenI | rs769455 |
| Biobank | rs769455 |
| 1000 genomes | rs769455 |
| hgdp | rs769455 |
| ensembl | rs769455 |
| geneview | rs769455 |
| scholar | rs769455 |
| rs769455 | |
| pharmgkb | rs769455 |
| gwascentral | rs769455 |
| openSNP | rs769455 |
| 23andMe | rs769455 |
| SNPshot | rs769455 |
| SNPdbe | rs769455 |
| MSV3d | rs769455 |
| GWAS Ctlg | rs769455 |
| GMAF | 0.009642 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
The ancestral allele is C.
| ClinVar | |
|---|---|
| Risk | rs769455(T;T) |
| Alt | rs769455(T;T) |
| Reference | Rs769455(C;C) |
| Significance | Pathogenic |
| Disease | Familial type 3 hyperlipoproteinemia |
| Variation | info |
| Gene | APOE |
| CLNDBN | Familial type 3 hyperlipoproteinemia |
| Reversed | 0 |
| HGVS | NC_000019.9:g.45412040C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019432.30, RCV000019443.28, |
[PMID 17658295] Association of ApoE genetic variants with obstructive sleep apnea in children.
[PMID 17672902
] Subarachnoid hemorrhage: tests of association with apolipoprotein E and elastin genes.
