rs757863
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs757863(A;A) |
| Make rs757863(A;G) |
| Make rs757863(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 78042064 |
| Gene | MAGI2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs757863 |
| dbSNP (classic) | rs757863 |
| ClinGen | rs757863 |
| ebi | rs757863 |
| HLI | rs757863 |
| Exac | rs757863 |
| Gnomad | rs757863 |
| Varsome | rs757863 |
| LitVar | rs757863 |
| Map | rs757863 |
| PheGenI | rs757863 |
| Biobank | rs757863 |
| 1000 genomes | rs757863 |
| hgdp | rs757863 |
| ensembl | rs757863 |
| geneview | rs757863 |
| scholar | rs757863 |
| rs757863 | |
| pharmgkb | rs757863 |
| gwascentral | rs757863 |
| openSNP | rs757863 |
| 23andMe | rs757863 |
| SNPshot | rs757863 |
| SNPdbe | rs757863 |
| MSV3d | rs757863 |
| GWAS Ctlg | rs757863 |
| GMAF | 0.3838 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients.[PMID 17671248]
