rs9270986
| Orientation | plus |
| Stabilized | plus |
| Make rs9270986(A;A) |
| Make rs9270986(A;C) |
| Make rs9270986(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32606283 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9270986 |
| dbSNP (classic) | rs9270986 |
| ClinGen | rs9270986 |
| ebi | rs9270986 |
| HLI | rs9270986 |
| Exac | rs9270986 |
| Gnomad | rs9270986 |
| Varsome | rs9270986 |
| LitVar | rs9270986 |
| Map | rs9270986 |
| PheGenI | rs9270986 |
| Biobank | rs9270986 |
| 1000 genomes | rs9270986 |
| hgdp | rs9270986 |
| ensembl | rs9270986 |
| geneview | rs9270986 |
| scholar | rs9270986 |
| rs9270986 | |
| pharmgkb | rs9270986 |
| gwascentral | rs9270986 |
| openSNP | rs9270986 |
| 23andMe | rs9270986 |
| SNPshot | rs9270986 |
| SNPdbe | rs9270986 |
| MSV3d | rs9270986 |
| GWAS Ctlg | rs9270986 |
| GMAF | 0.1561 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| Rs9270986 | |
|---|---|
| PubMed | [PMID 17554300 |
| Affy Probeset | SNP_A-1837012 |
| Affy Orientation | same |
| On GW 5.0 | 0 |
| Alleles A/B | A/C |
| Ancestral | C |
| Population | |
| Allele | |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | |
| Disease | Type I Diabetes (T1D) |
[PMID 20639878] A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury
This SNP is associated with a higher risk of liver injury in patients taking the nonsteroidal anti-inflammatory drug lumiracoxib, which has been withdrawn from most markets.
[PMID 17660530] Risk alleles for multiple sclerosis identified by a genomewide study.
[PMID 19956648
] Pathway analysis of GWAS provides new insights into genetic susceptibility to 3 inflammatory diseases.
[PMID 20045101
] Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.
[PMID 20546594
] An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings.
[PMID 22495925] Genetic polymorphisms inside and outside the MHC improve prediction of AS radiographic severity in addition to clinical variables.
[PMID 26083016] Accuracy of SNPs to predict risk of HLA alleles associated with drug-induced hypersensitivity events across racial groups
- Is a snp
- In dbSNP
- SNPs on chromosome 6
- Has genotype
- Has population
- Has Report GE
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Affy500k
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
