rs9275390
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9275390(C;C) |
| Make rs9275390(C;T) |
| Make rs9275390(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32701379 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9275390 |
| dbSNP (classic) | rs9275390 |
| ClinGen | rs9275390 |
| ebi | rs9275390 |
| HLI | rs9275390 |
| Exac | rs9275390 |
| Gnomad | rs9275390 |
| Varsome | rs9275390 |
| LitVar | rs9275390 |
| Map | rs9275390 |
| PheGenI | rs9275390 |
| Biobank | rs9275390 |
| 1000 genomes | rs9275390 |
| hgdp | rs9275390 |
| ensembl | rs9275390 |
| geneview | rs9275390 |
| scholar | rs9275390 |
| rs9275390 | |
| pharmgkb | rs9275390 |
| gwascentral | rs9275390 |
| openSNP | rs9275390 |
| 23andMe | rs9275390 |
| SNPshot | rs9275390 |
| SNPdbe | rs9275390 |
| MSV3d | rs9275390 |
| GWAS Ctlg | rs9275390 |
| GMAF | 0.3136 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21779181 ]
|
| Trait | |
| Title | Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. |
| Risk Allele | |
| P-val | 1E-7 |
| Odds Ratio | 1.6100 [1.35-1.92] |
[PMID 19458352] Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.
