rs13133980
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs13133980(C;G) |
| Make rs13133980(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 41000929 |
| Gene | APBB2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13133980 |
| dbSNP (classic) | rs13133980 |
| ClinGen | rs13133980 |
| ebi | rs13133980 |
| HLI | rs13133980 |
| Exac | rs13133980 |
| Gnomad | rs13133980 |
| Varsome | rs13133980 |
| LitVar | rs13133980 |
| Map | rs13133980 |
| PheGenI | rs13133980 |
| Biobank | rs13133980 |
| 1000 genomes | rs13133980 |
| hgdp | rs13133980 |
| ensembl | rs13133980 |
| geneview | rs13133980 |
| scholar | rs13133980 |
| rs13133980 | |
| pharmgkb | rs13133980 |
| gwascentral | rs13133980 |
| openSNP | rs13133980 |
| 23andMe | rs13133980 |
| SNPshot | rs13133980 |
| SNPdbe | rs13133980 |
| MSV3d | rs13133980 |
| GWAS Ctlg | rs13133980 |
| GMAF | 0.4986 |
| Max Magnitude | 0 |
[PMID 18852029] Analysis of APBB2 gene polymorphisms in sporadic Alzheimer's disease.
| OMIM | 602710 |
| Desc | AMYLOID BETA A4 PRECURSOR PROTEIN-BINDING, FAMILY B, MEMBER 2; APBB2 |
| Variant | |
| Related | also |
[PMID 15714520] Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease.
[PMID 23384821] APBB2 genetic polymorphisms are associated with severe cognitive impairment in centenarians.
