rs3823355
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3823355(C;C) |
| Make rs3823355(C;T) |
| Make rs3823355(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 29974306 |
| Gene | HCG9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3823355 |
| dbSNP (classic) | rs3823355 |
| ClinGen | rs3823355 |
| ebi | rs3823355 |
| HLI | rs3823355 |
| Exac | rs3823355 |
| Gnomad | rs3823355 |
| Varsome | rs3823355 |
| LitVar | rs3823355 |
| Map | rs3823355 |
| PheGenI | rs3823355 |
| Biobank | rs3823355 |
| 1000 genomes | rs3823355 |
| hgdp | rs3823355 |
| ensembl | rs3823355 |
| geneview | rs3823355 |
| scholar | rs3823355 |
| rs3823355 | |
| pharmgkb | rs3823355 |
| gwascentral | rs3823355 |
| openSNP | rs3823355 |
| 23andMe | rs3823355 |
| SNPshot | rs3823355 |
| SNPdbe | rs3823355 |
| MSV3d | rs3823355 |
| GWAS Ctlg | rs3823355 |
| GMAF | 0.2805 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19010793
] Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
[PMID 20593013] A major histocompatibility Class I locus contributes to multiple sclerosis susceptibility independently from HLA-DRB1*15:01.
| GWAS snp | |
|---|---|
| PMID | [PMID 20410501]
|
| Trait | Vitiligo |
| Title | Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. |
| Risk Allele | T |
| P-val | 9E-23 |
| Odds Ratio | 1.50 [1.39-1.63] |
