rs2503875
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2503875(A;A) |
| Make rs2503875(A;G) |
| Make rs2503875(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 43318601 |
| Gene | LOC105378271 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2503875 |
| dbSNP (classic) | rs2503875 |
| ClinGen | rs2503875 |
| ebi | rs2503875 |
| HLI | rs2503875 |
| Exac | rs2503875 |
| Gnomad | rs2503875 |
| Varsome | rs2503875 |
| LitVar | rs2503875 |
| Map | rs2503875 |
| PheGenI | rs2503875 |
| Biobank | rs2503875 |
| 1000 genomes | rs2503875 |
| hgdp | rs2503875 |
| ensembl | rs2503875 |
| geneview | rs2503875 |
| scholar | rs2503875 |
| rs2503875 | |
| pharmgkb | rs2503875 |
| gwascentral | rs2503875 |
| openSNP | rs2503875 |
| 23andMe | rs2503875 |
| SNPshot | rs2503875 |
| SNPdbe | rs2503875 |
| MSV3d | rs2503875 |
| GWAS Ctlg | rs2503875 |
| GMAF | 0.286 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20598377] |
| Trait | Multiple sclerosis |
| Title | Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis |
| Risk Allele | A |
| P-val | 2E-7 |
| Odds Ratio | 1.66 [1.37-2.00] |
[PMID 20532249
] Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.
