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rs10494879

From SNPedia

Orientationplus
Stabilizedplus
Make rs10494879(C;C)
Make rs10494879(C;G)
Make rs10494879(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position206778859
is asnp
is mentioned by
dbSNPrs10494879
ebirs10494879
HLIrs10494879
Exacrs10494879
Varsomers10494879
Maprs10494879
PheGenIrs10494879
hapmaprs10494879
1000 genomesrs10494879
hgdprs10494879
ensemblrs10494879
gopubmedrs10494879
geneviewrs10494879
scholarrs10494879
googlers10494879
pharmgkbrs10494879
gwascentralrs10494879
openSNPrs10494879
23andMers10494879
23andMe allrs10494879
SNP Nexus

SNPshotrs10494879
SNPdbers10494879
MSV3drs10494879
GWAS Ctlgrs10494879
GMAF0.2658
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 23299779OA-icon.png] Interleukin-10 gene polymorphisms are associated with freedom from treatment failure for patients with Hodgkin lymphoma


[PMID 17903307OA-icon.png] Framingham Heart Study genome-wide association: results for pulmonary function measures.


[PMID 18559596] Effect of interleukin-10 gene polymorphisms on clinical outcome of patients with aggressive non-Hodgkin's lymphoma: an exploratory study.


[PMID 19852851OA-icon.png] Asthma and genes encoding components of the vitamin D pathway.