rs1841770
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1841770(G;G) |
| Make rs1841770(G;T) |
| Make rs1841770(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 148038899 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1841770 |
| dbSNP (classic) | rs1841770 |
| ClinGen | rs1841770 |
| ebi | rs1841770 |
| HLI | rs1841770 |
| Exac | rs1841770 |
| Gnomad | rs1841770 |
| Varsome | rs1841770 |
| LitVar | rs1841770 |
| Map | rs1841770 |
| PheGenI | rs1841770 |
| Biobank | rs1841770 |
| 1000 genomes | rs1841770 |
| hgdp | rs1841770 |
| ensembl | rs1841770 |
| geneview | rs1841770 |
| scholar | rs1841770 |
| rs1841770 | |
| pharmgkb | rs1841770 |
| gwascentral | rs1841770 |
| openSNP | rs1841770 |
| 23andMe | rs1841770 |
| SNPshot | rs1841770 |
| SNPdbe | rs1841770 |
| MSV3d | rs1841770 |
| GWAS Ctlg | rs1841770 |
| GMAF | 0.2902 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 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 | 0.000008 |
| Odds Ratio | 1.34 [NR] |
[PMID 20944657] Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.
[PMID 22411505] Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients.
