rs1790100
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1790100(G;G) |
| Make rs1790100(G;T) |
| Make rs1790100(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 123172178 |
| Gene | MPHOSPH9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1790100 |
| dbSNP (classic) | rs1790100 |
| ClinGen | rs1790100 |
| ebi | rs1790100 |
| HLI | rs1790100 |
| Exac | rs1790100 |
| Gnomad | rs1790100 |
| Varsome | rs1790100 |
| LitVar | rs1790100 |
| Map | rs1790100 |
| PheGenI | rs1790100 |
| Biobank | rs1790100 |
| 1000 genomes | rs1790100 |
| hgdp | rs1790100 |
| ensembl | rs1790100 |
| geneview | rs1790100 |
| scholar | rs1790100 |
| rs1790100 | |
| pharmgkb | rs1790100 |
| gwascentral | rs1790100 |
| openSNP | rs1790100 |
| 23andMe | rs1790100 |
| SNPshot | rs1790100 |
| SNPdbe | rs1790100 |
| MSV3d | rs1790100 |
| GWAS Ctlg | rs1790100 |
| GMAF | 0.3136 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19525953 ]
|
| Trait | Multiple sclerosis |
| Title | Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci |
| Risk Allele | G |
| P-val | 7E-7 |
| Odds Ratio | 1.11 [1.00-1.22] |
