rs397020
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs397020(A;A) |
| Make rs397020(A;G) |
| Make rs397020(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 20 |
| Position | 1225242 |
| Gene | RAD21L1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs397020 |
| dbSNP (classic) | rs397020 |
| ClinGen | rs397020 |
| ebi | rs397020 |
| HLI | rs397020 |
| Exac | rs397020 |
| Gnomad | rs397020 |
| Varsome | rs397020 |
| LitVar | rs397020 |
| Map | rs397020 |
| PheGenI | rs397020 |
| Biobank | rs397020 |
| 1000 genomes | rs397020 |
| hgdp | rs397020 |
| ensembl | rs397020 |
| geneview | rs397020 |
| scholar | rs397020 |
| rs397020 | |
| pharmgkb | rs397020 |
| gwascentral | rs397020 |
| openSNP | rs397020 |
| 23andMe | rs397020 |
| SNPshot | rs397020 |
| SNPdbe | rs397020 |
| MSV3d | rs397020 |
| GWAS Ctlg | rs397020 |
| GMAF | 0.4711 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19010793 ]
|
| Trait | Multiple sclerosis |
| Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
| Risk Allele | |
| P-val | 8E-7 |
| Odds Ratio | 1.41 [NR] |
[PMID 20944657] Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.
