rs28930977
From SNPedia
| Merged into | rs121917808 |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs28930977(A;A) |
| Make rs28930977(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 73219192 |
| Gene | PSEN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28930977 |
| dbSNP (classic) | rs28930977 |
| ClinGen | rs28930977 |
| ebi | rs28930977 |
| HLI | rs28930977 |
| Exac | rs28930977 |
| Gnomad | rs28930977 |
| Varsome | rs28930977 |
| LitVar | rs28930977 |
| Map | rs28930977 |
| PheGenI | rs28930977 |
| Biobank | rs28930977 |
| 1000 genomes | rs28930977 |
| hgdp | rs28930977 |
| ensembl | rs28930977 |
| geneview | rs28930977 |
| scholar | rs28930977 |
| rs28930977 | |
| pharmgkb | rs28930977 |
| gwascentral | rs28930977 |
| openSNP | rs28930977 |
| 23andMe | rs28930977 |
| SNPshot | rs28930977 |
| SNPdbe | rs28930977 |
| MSV3d | rs28930977 |
| GWAS Ctlg | rs28930977 |
| Status | Merged into rs121917808 |
| Max Magnitude | 0 |
Variations in this snp are related to ALZHEIMER DISEASE, FAMILIAL, 3 Omim 607822. Dementia, SPASTIC PARAPARESIS, APRAXIA,
