rs2069827
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 |
Make rs2069827(G;T) |
Make rs2069827(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 22725837 |
Gene | IL6, LOC541472 |
is a | snp |
is | mentioned by |
dbSNP | rs2069827 |
dbSNP (classic) | rs2069827 |
ClinGen | rs2069827 |
ebi | rs2069827 |
HLI | rs2069827 |
Exac | rs2069827 |
Gnomad | rs2069827 |
Varsome | rs2069827 |
LitVar | rs2069827 |
Map | rs2069827 |
PheGenI | rs2069827 |
Biobank | rs2069827 |
1000 genomes | rs2069827 |
hgdp | rs2069827 |
ensembl | rs2069827 |
geneview | rs2069827 |
scholar | rs2069827 |
rs2069827 | |
pharmgkb | rs2069827 |
gwascentral | rs2069827 |
openSNP | rs2069827 |
23andMe | rs2069827 |
SNPshot | rs2069827 |
SNPdbe | rs2069827 |
MSV3d | rs2069827 |
GWAS Ctlg | rs2069827 |
GMAF | 0.04775 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 19280716] The IL6-174G/C polymorphism is associated with celiac disease susceptibility in girls.
[PMID 21889771] Lack of association between IL6 single nucleotide polymorphisms and cardiovascular disease in Spanish patients with rheumatoid arthritis
[PMID 22234866] Evidence from case-control and longitudinal studies supports associations of genetic variation in APOE, CETP, and IL6 with human longevity.
[PMID 16644865] Genetic variation in IL6 gene and type 2 diabetes: tagging-SNP haplotype analysis in large-scale case-control study and meta-analysis.
[PMID 17623760] Interleukin-6 genetic variability and adiposity: associations in two prospective cohorts and systematic review in 26,944 individuals.
[PMID 17847004] Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance.
[PMID 18420533] The effect of IL6-174C/G polymorphism on postprandial triglyceride metabolism in the GOLDN studyboxs.
[PMID 18496509] An IL-6 haplotype on human chromosome 7p21 confers risk for impaired renal function in type 2 diabetic patients.
[PMID 18781131] Interleukin and interleukin receptor gene polymorphisms and susceptibility to melanoma.
[PMID 19272152] IL6 and CRP haplotypes are associated with COPD risk and systemic inflammation: a case-control study.
[PMID 19359268] Associations of IL6 polymorphisms with lung function decline and COPD.
[PMID 19387461] Interleukin-6 haplotypes and the response to therapy of chronic hepatitis C virus infection.
[PMID 23027890] Influence of the IL6 gene in susceptibility to systemic sclerosis.
[PMID 23459936] Exploring the genetic basis of chronic periodontitis: a genome-wide association study.
[PMID 31082334] [Correlation between interleukin-6 single nucleotide polymorphism and the occurrence and prognosis of hepatitis B virus-associated acute-on-chronic liver failure].
- Is a snp
- In dbSNP
- SNPs on chromosome 7
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2c
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2d