rs63750151
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;G) | 7 | Alzheimer's disease |
| (G;G) | 0 | common/normal |
| Make rs63750151(C;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 21 |
| Position | 25891761 |
| Gene | APP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs63750151 |
| dbSNP (classic) | rs63750151 |
| ClinGen | rs63750151 |
| ebi | rs63750151 |
| HLI | rs63750151 |
| Exac | rs63750151 |
| Gnomad | rs63750151 |
| Varsome | rs63750151 |
| LitVar | rs63750151 |
| Map | rs63750151 |
| PheGenI | rs63750151 |
| Biobank | rs63750151 |
| 1000 genomes | rs63750151 |
| hgdp | rs63750151 |
| ensembl | rs63750151 |
| geneview | rs63750151 |
| scholar | rs63750151 |
| rs63750151 | |
| pharmgkb | rs63750151 |
| gwascentral | rs63750151 |
| openSNP | rs63750151 |
| 23andMe | rs63750151 |
| SNPshot | rs63750151 |
| SNPdbe | rs63750151 |
| MSV3d | rs63750151 |
| GWAS Ctlg | rs63750151 |
| Max Magnitude | 7 |
aka Lys724Asn or K724N
| ClinVar | |
|---|---|
| Risk | rs63750151(C;C) |
| Alt | rs63750151(C;C) |
| Reference | Rs63750151(G;G) |
| Significance | Untested |
| Disease | not provided |
| Variation | info |
| Gene | APP |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000021.8:g.27264073C>G |
| CLNSRC | |
| CLNACC | RCV000084578.1, |
