rs4727380
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4727380(C;C) |
| Make rs4727380(C;G) |
| Make rs4727380(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 77416489 |
| Gene | GSAP, LOC101927243 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4727380 |
| dbSNP (classic) | rs4727380 |
| ClinGen | rs4727380 |
| ebi | rs4727380 |
| HLI | rs4727380 |
| Exac | rs4727380 |
| Gnomad | rs4727380 |
| Varsome | rs4727380 |
| LitVar | rs4727380 |
| Map | rs4727380 |
| PheGenI | rs4727380 |
| Biobank | rs4727380 |
| 1000 genomes | rs4727380 |
| hgdp | rs4727380 |
| ensembl | rs4727380 |
| geneview | rs4727380 |
| scholar | rs4727380 |
| rs4727380 | |
| pharmgkb | rs4727380 |
| gwascentral | rs4727380 |
| openSNP | rs4727380 |
| 23andMe | rs4727380 |
| SNPshot | rs4727380 |
| SNPdbe | rs4727380 |
| MSV3d | rs4727380 |
| GWAS Ctlg | rs4727380 |
| Max Magnitude | 0 |
[PMID 25037285] A common GSAP promoter variant contributes to Alzheimer's disease liability
