rs10136766
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10136766(A;A) |
| Make rs10136766(A;G) |
| Make rs10136766(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 105766248 |
| Gene | LOC105378184 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10136766 |
| dbSNP (classic) | rs10136766 |
| ClinGen | rs10136766 |
| ebi | rs10136766 |
| HLI | rs10136766 |
| Exac | rs10136766 |
| Gnomad | rs10136766 |
| Varsome | rs10136766 |
| LitVar | rs10136766 |
| Map | rs10136766 |
| PheGenI | rs10136766 |
| Biobank | rs10136766 |
| 1000 genomes | rs10136766 |
| hgdp | rs10136766 |
| ensembl | rs10136766 |
| geneview | rs10136766 |
| scholar | rs10136766 |
| rs10136766 | |
| pharmgkb | rs10136766 |
| gwascentral | rs10136766 |
| openSNP | rs10136766 |
| 23andMe | rs10136766 |
| SNPshot | rs10136766 |
| SNPdbe | rs10136766 |
| MSV3d | rs10136766 |
| GWAS Ctlg | rs10136766 |
| GMAF | 0.2897 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 23225573 ]
|
| Trait | IgG levels |
| Title | Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis. |
| Risk Allele | A |
| P-val | 8E-16 |
| Odds Ratio | .23 [NR] unit increase |
