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rs4901706

From SNPedia

Orientationplus
Stabilizedplus
Make rs4901706(A;A)
Make rs4901706(A;G)
Make rs4901706(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position56647667
GeneTMEM260
is asnp
is mentioned by
dbSNPrs4901706
ebirs4901706
HLIrs4901706
Exacrs4901706
Varsomers4901706
Maprs4901706
PheGenIrs4901706
hapmaprs4901706
1000 genomesrs4901706
hgdprs4901706
ensemblrs4901706
gopubmedrs4901706
geneviewrs4901706
scholarrs4901706
googlers4901706
pharmgkbrs4901706
gwascentralrs4901706
openSNPrs4901706
23andMers4901706
23andMe allrs4901706
SNP Nexus

SNPshotrs4901706
SNPdbers4901706
MSV3drs4901706
GWAS Ctlgrs4901706
GMAF0.1667
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24530479] A miR-SNP of the KRT81 gene is associated with the prognosis of non-Hodgkin's lymphoma


[PMID 17584784OA-icon.png] Aberrant allele frequencies of the SNPs located in microRNA target sites are potentially associated with human cancers.


[PMID 24831772] A polymorphism at the microRNA binding site in the 3' untranslated region of C14orf101 is associated with non-Hodgkin lymphoma overall survival


[PMID 26309413OA-icon.png] A polymorphism at the microRNA binding site in the 3' untranslated region of RYR3 is associated with outcome in hepatocellular carcinoma


[PMID 27602096] A polymorphism at the microRNA binding site in the 3'-untranslated region of C14orf101 is associated with the risk of gastric cancer development.