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a higher risk of liver injury in patients taking the nonsteroidal anti-inflammatory drug lumiracoxib, which has been withdrawn from most markets.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