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rs2056576

From SNPedia

Orientationplus
Stabilizedplus
Make rs2056576(C;C)
Make rs2056576(C;T)
Make rs2056576(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position22721583
is asnp
is mentioned by
dbSNPrs2056576
ebirs2056576
HLIrs2056576
Exacrs2056576
Varsomers2056576
Maprs2056576
PheGenIrs2056576
hapmaprs2056576
1000 genomesrs2056576
hgdprs2056576
ensemblrs2056576
gopubmedrs2056576
geneviewrs2056576
scholarrs2056576
googlers2056576
pharmgkbrs2056576
gwascentralrs2056576
openSNPrs2056576
23andMers2056576
23andMe allrs2056576
SNP Nexus

SNPshotrs2056576
SNPdbers2056576
MSV3drs2056576
GWAS Ctlgrs2056576
GMAF0.2599
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21997388] Mendelian Randomization Study of Interleukin-6 in Chronic Obstructive Pulmonary Disease


[PMID 17847004OA-icon.png] Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance.


[PMID 18194558OA-icon.png] A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples.


[PMID 19387461OA-icon.png] Interleukin-6 haplotypes and the response to therapy of chronic hepatitis C virus infection.