rs12047808
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12047808(A;A) |
| Make rs12047808(A;G) |
| Make rs12047808(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 179500179 |
| Gene | AXDND1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12047808 |
| dbSNP (classic) | rs12047808 |
| ClinGen | rs12047808 |
| ebi | rs12047808 |
| HLI | rs12047808 |
| Exac | rs12047808 |
| Gnomad | rs12047808 |
| Varsome | rs12047808 |
| LitVar | rs12047808 |
| Map | rs12047808 |
| PheGenI | rs12047808 |
| Biobank | rs12047808 |
| 1000 genomes | rs12047808 |
| hgdp | rs12047808 |
| ensembl | rs12047808 |
| geneview | rs12047808 |
| scholar | rs12047808 |
| rs12047808 | |
| pharmgkb | rs12047808 |
| gwascentral | rs12047808 |
| openSNP | rs12047808 |
| 23andMe | rs12047808 |
| SNPshot | rs12047808 |
| SNPdbe | rs12047808 |
| MSV3d | rs12047808 |
| GWAS Ctlg | rs12047808 |
| GMAF | 0.1538 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19010793 ]
|
| Trait | Multiple sclerosis (age of onset) |
| Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | NR NR |
