rs850713
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs850713(C;C) |
| Make rs850713(C;T) |
| Make rs850713(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 44350364 |
| Gene | GRN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs850713 |
| dbSNP (classic) | rs850713 |
| ClinGen | rs850713 |
| ebi | rs850713 |
| HLI | rs850713 |
| Exac | rs850713 |
| Gnomad | rs850713 |
| Varsome | rs850713 |
| LitVar | rs850713 |
| Map | rs850713 |
| PheGenI | rs850713 |
| Biobank | rs850713 |
| 1000 genomes | rs850713 |
| hgdp | rs850713 |
| ensembl | rs850713 |
| geneview | rs850713 |
| scholar | rs850713 |
| rs850713 | |
| pharmgkb | rs850713 |
| gwascentral | rs850713 |
| openSNP | rs850713 |
| 23andMe | rs850713 |
| SNPshot | rs850713 |
| SNPdbe | rs850713 |
| MSV3d | rs850713 |
| GWAS Ctlg | rs850713 |
| GMAF | 0.3343 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
Associated with risk of amyotrophic lateral sclerosis (ALS) in two European populations [PMID 18184915]
[PMID 19016491] An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population.
[PMID 19625741
] Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.
[PMID 19640594] Recent insights into the molecular genetics of dementia.
