rs5937496
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5937496(A;A) |
| Make rs5937496(A;G) |
| Make rs5937496(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 76127599 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5937496 |
| dbSNP (classic) | rs5937496 |
| ClinGen | rs5937496 |
| ebi | rs5937496 |
| HLI | rs5937496 |
| Exac | rs5937496 |
| Gnomad | rs5937496 |
| Varsome | rs5937496 |
| LitVar | rs5937496 |
| Map | rs5937496 |
| PheGenI | rs5937496 |
| Biobank | rs5937496 |
| 1000 genomes | rs5937496 |
| hgdp | rs5937496 |
| ensembl | rs5937496 |
| geneview | rs5937496 |
| scholar | rs5937496 |
| rs5937496 | |
| pharmgkb | rs5937496 |
| gwascentral | rs5937496 |
| openSNP | rs5937496 |
| 23andMe | rs5937496 |
| SNPshot | rs5937496 |
| SNPdbe | rs5937496 |
| MSV3d | rs5937496 |
| GWAS Ctlg | rs5937496 |
| GMAF | 0.1179 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19734901] |
| Trait | Amyotrophic lateral sclerosis |
| Title | Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis |
| Risk Allele | |
| P-val | 6E-7 |
| Odds Ratio | 1.38 [NR] |
