rs4792938
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4792938(C;C) |
| Make rs4792938(C;G) |
| Make rs4792938(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 44347231 |
| Gene | GRN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4792938 |
| dbSNP (classic) | rs4792938 |
| ClinGen | rs4792938 |
| ebi | rs4792938 |
| HLI | rs4792938 |
| Exac | rs4792938 |
| Gnomad | rs4792938 |
| Varsome | rs4792938 |
| LitVar | rs4792938 |
| Map | rs4792938 |
| PheGenI | rs4792938 |
| Biobank | rs4792938 |
| 1000 genomes | rs4792938 |
| hgdp | rs4792938 |
| ensembl | rs4792938 |
| geneview | rs4792938 |
| scholar | rs4792938 |
| rs4792938 | |
| pharmgkb | rs4792938 |
| gwascentral | rs4792938 |
| openSNP | rs4792938 |
| 23andMe | rs4792938 |
| SNPshot | rs4792938 |
| SNPdbe | rs4792938 |
| MSV3d | rs4792938 |
| GWAS Ctlg | rs4792938 |
| GMAF | 0.4086 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20061636] GRN variability contributes to sporadic frontotemporal lobar degeneration [PMID 20463744] Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males.
[PMID 24581833] Further evidence for plasma progranulin as a biomarker in bipolar disorder
