rs137852703
From SNPedia
| Merged into | rs28936380 |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;G) | ||
| (G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 226885546 |
| Gene | PSEN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137852703 |
| dbSNP (classic) | rs137852703 |
| ClinGen | rs137852703 |
| ebi | rs137852703 |
| HLI | rs137852703 |
| Exac | rs137852703 |
| Gnomad | rs137852703 |
| Varsome | rs137852703 |
| LitVar | rs137852703 |
| Map | rs137852703 |
| PheGenI | rs137852703 |
| Biobank | rs137852703 |
| 1000 genomes | rs137852703 |
| hgdp | rs137852703 |
| ensembl | rs137852703 |
| geneview | rs137852703 |
| scholar | rs137852703 |
| rs137852703 | |
| pharmgkb | rs137852703 |
| gwascentral | rs137852703 |
| openSNP | rs137852703 |
| 23andMe | rs137852703 |
| SNPshot | rs137852703 |
| SNPdbe | rs137852703 |
| MSV3d | rs137852703 |
| GWAS Ctlg | rs137852703 |
| Status | Merged into rs28936380 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | Rs137852703(G;G) |
| Alt | Rs137852703(G;G) |
| Reference | Rs137852703(C;C) |
| Significance | Pathogenic |
| Disease | Alzheimer disease |
| Variation | info |
| Gene | PSEN2 |
| CLNDBN | Alzheimer disease, type 4 |
| Reversed | 0 |
| HGVS | NC_000001.10:g.227073247C>G |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | SCV000029617.1, |
