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rs8126

From SNPedia

Orientationplus
Stabilizedplus
Make rs8126(C;C)
Make rs8126(C;T)
Make rs8126(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position103137232
GeneTNFAIP2
is asnp
is mentioned by
dbSNPrs8126
ebirs8126
HLIrs8126
Exacrs8126
Varsomers8126
Maprs8126
PheGenIrs8126
hapmaprs8126
1000 genomesrs8126
hgdprs8126
ensemblrs8126
gopubmedrs8126
geneviewrs8126
scholarrs8126
googlers8126
pharmgkbrs8126
gwascentralrs8126
openSNPrs8126
23andMers8126
23andMe allrs8126
SNP Nexus

SNPshotrs8126
SNPdbers8126
MSV3drs8126
GWAS Ctlgrs8126
GMAF0.3737
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21934093OA-icon.png] A Functional Variant at the miR-184 Binding Site in TNFAIP2 and Risk of Squamous Cell Carcinoma of the Head and Neck


[PMID 23724109OA-icon.png] The miR-184 Binding-Site rs8126 T>C Polymorphism in TNFAIP2 Is Associated with Risk of Gastric Cancer


[PMID 25383966OA-icon.png] A Functional TNFAIP2 3'-UTR rs8126 Genetic Polymorphism Contributes to Risk of Esophageal Squamous Cell Carcinoma