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rs16917496

From SNPedia

Orientationplus
Stabilizedplus
Make rs16917496(C;C)
Make rs16917496(C;T)
Make rs16917496(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position123409283
GeneSETD8
is asnp
is mentioned by
dbSNPrs16917496
ebirs16917496
HLIrs16917496
Exacrs16917496
Varsomers16917496
Maprs16917496
PheGenIrs16917496
hapmaprs16917496
1000 genomesrs16917496
hgdprs16917496
ensemblrs16917496
gopubmedrs16917496
geneviewrs16917496
scholarrs16917496
googlers16917496
pharmgkbrs16917496
gwascentralrs16917496
openSNPrs16917496
23andMers16917496
23andMe allrs16917496
SNP Nexus

SNPshotrs16917496
SNPdbers16917496
MSV3drs16917496
GWAS Ctlgrs16917496
GMAF0.4692
Max Magnitude

[PMID 22095217] A polymorphism at the miR-502 binding site in the 3' untranslated region of the histone methyltransferase SET8 is associated with hepatocellular carcinoma outcome

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


[PMID 23291132] [SNP rs16917496 within SET8 3'UTR is associated with the age of onset of breast cancer]


[PMID 27346408] [Polymorphism at the miR-502 binding site in the 3' untranslated region of SET8 gene is associated with the risk of clear cell renal cell carcinoma].

[PMID 27605386] miR-502 medaited histone methyltransferase SET8 expression is associated with outcome of esophageal squamous cell carcinoma.