rs6587852
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs6587852(A;A) |
| Make rs6587852(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 59239775 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6587852 |
| dbSNP (classic) | rs6587852 |
| ClinGen | rs6587852 |
| ebi | rs6587852 |
| HLI | rs6587852 |
| Exac | rs6587852 |
| Gnomad | rs6587852 |
| Varsome | rs6587852 |
| LitVar | rs6587852 |
| Map | rs6587852 |
| PheGenI | rs6587852 |
| Biobank | rs6587852 |
| 1000 genomes | rs6587852 |
| hgdp | rs6587852 |
| ensembl | rs6587852 |
| geneview | rs6587852 |
| scholar | rs6587852 |
| rs6587852 | |
| pharmgkb | rs6587852 |
| gwascentral | rs6587852 |
| openSNP | rs6587852 |
| 23andMe | rs6587852 |
| SNPshot | rs6587852 |
| SNPdbe | rs6587852 |
| MSV3d | rs6587852 |
| GWAS Ctlg | rs6587852 |
| GMAF | 0.225 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
rs6587852 is one of 6 SNPs found upstream of an (uncharacterized) gene known as FLJ10986 that have been found to be overrepresented in 1,152 patients with sporadic amyotrophic lateral sclerosis (ALS).[PMID 17671248]
[PMID 19177248] A study involving a large case-control series from the Netherlands, Belgium, Sweden and Ireland (total: 1883 sporadic ALS patients and 2063 controls) found no significant association between sporadic ALS and the six previously reported associated SNPs, including this one.
[PMID 19922138] Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis
