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rs1800797

From SNPedia

Orientationplus
Stabilizedplus
Make rs1800797(A;A)
Make rs1800797(A;G)
Make rs1800797(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position22726602
GeneIL6, LOC541472
is asnp
is mentioned by
dbSNPrs1800797
dbSNP (classic)rs1800797
ClinGenrs1800797
ebirs1800797
HLIrs1800797
Exacrs1800797
Gnomadrs1800797
Varsomers1800797
LitVarrs1800797
Maprs1800797
PheGenIrs1800797
Biobankrs1800797
1000 genomesrs1800797
hgdprs1800797
ensemblrs1800797
geneviewrs1800797
scholarrs1800797
googlers1800797
pharmgkbrs1800797
gwascentralrs1800797
openSNPrs1800797
23andMers1800797
SNPshotrs1800797
SNPdbers1800797
MSV3drs1800797
GWAS Ctlgrs1800797
GMAF0.1818
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 18257935OA-icon.png] rs1800797, rs1800796 and rs1800795 have been shown to affect both the transcription and secretion of IL-6, to symptomatic distal interphalangeal osteoarthritis based on 535 women. the G alleles of two promoter single-nucleotide polymorphisms (SNP) G-597A and G-174C were more common among the subjects with symptomatic DIP OA than among those with no disease (p-values corrected for multiple testing 0.020 and 0.024). Also, the carriage of at least one G allele in these positions increased the risk of disease (p=0.006 and, p=0.008, respectively). Carrying a haplotype with the G allele in all three promoter SNPs increased the risk of symptomatic DIP OA more than four-fold (OR 4.45, p=0.001). Carriage of the G-G diplotype indicated an increased risk of both symmetrical DIP OA (OR 1.52 95% CI 1.01 to 2.28) and symptomatic DIP OA (OR 3.67 95% CI 1.50 to 9.00)

[PMID 18449426] rs1800797 coronary artery disease 190 affected Asian Indian sibling pairs


[PMID 19435922OA-icon.png] Host genetic variants in the interleukin-6 promoter predict poor outcome in patients with estrogen receptor-positive, node-positive breast cancer

OMIM147620
DescINTERLEUKIN 6; IL6
Variant
Relatedalso

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