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rs10499563

From SNPedia

Orientationplus
Make rs10499563(C;C)
Make rs10499563(C;T)
Make rs10499563(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position22720869
is asnp
is mentioned by
dbSNPrs10499563
ebirs10499563
HLIrs10499563
Exacrs10499563
Varsomers10499563
Maprs10499563
PheGenIrs10499563
hapmaprs10499563
1000 genomesrs10499563
hgdprs10499563
ensemblrs10499563
gopubmedrs10499563
geneviewrs10499563
scholarrs10499563
googlers10499563
pharmgkbrs10499563
gwascentralrs10499563
openSNPrs10499563
23andMers10499563
23andMe allrs10499563
SNP Nexus

SNPshotrs10499563
SNPdbers10499563
MSV3drs10499563
GWAS Ctlgrs10499563
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 24776844] Associations between functional polymorphisms in the NFκB signaling pathway and response to anti-TNF treatment in Danish patients with inflammatory bowel disease

[PMID 26813132] [Association of single nucleotide polymorphisms of IL-6 gene with longevity in Uyghurs in Xinjiang].