rs63750363
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs63750363(C;C) |
| Make rs63750363(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 25897642 |
| Gene | APP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs63750363 |
| dbSNP (classic) | rs63750363 |
| ClinGen | rs63750363 |
| ebi | rs63750363 |
| HLI | rs63750363 |
| Exac | rs63750363 |
| Gnomad | rs63750363 |
| Varsome | rs63750363 |
| LitVar | rs63750363 |
| Map | rs63750363 |
| PheGenI | rs63750363 |
| Biobank | rs63750363 |
| 1000 genomes | rs63750363 |
| hgdp | rs63750363 |
| ensembl | rs63750363 |
| geneview | rs63750363 |
| scholar | rs63750363 |
| rs63750363 | |
| pharmgkb | rs63750363 |
| gwascentral | rs63750363 |
| openSNP | rs63750363 |
| 23andMe | rs63750363 |
| SNPshot | rs63750363 |
| SNPdbe | rs63750363 |
| MSV3d | rs63750363 |
| GWAS Ctlg | rs63750363 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs63750363(C;C) |
| Alt | rs63750363(C;C) |
| Reference | Rs63750363(G;G) |
| Significance | Pathogenic |
| Disease | Alzheimer disease not provided not specified |
| Variation | info |
| Gene | APP |
| CLNDBN | Alzheimer disease, type 1 not provided not specified |
| Reversed | 1 |
| HGVS | NC_000021.8:g.27269954C>G |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019722.27, RCV000084557.1, RCV000480114.1, |
