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rs1053667

From SNPedia

Orientationplus
Stabilizedplus
Make rs1053667(C;C)
Make rs1053667(C;T)
Make rs1053667(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position45073835
GeneFAM179B
is asnp
is mentioned by
dbSNPrs1053667
ebirs1053667
HLIrs1053667
Exacrs1053667
Varsomers1053667
Maprs1053667
PheGenIrs1053667
hapmaprs1053667
1000 genomesrs1053667
hgdprs1053667
ensemblrs1053667
gopubmedrs1053667
geneviewrs1053667
scholarrs1053667
googlers1053667
pharmgkbrs1053667
gwascentralrs1053667
openSNPrs1053667
23andMers1053667
23andMe allrs1053667
SNP Nexus

SNPshotrs1053667
SNPdbers1053667
MSV3drs1053667
GWAS Ctlgrs1053667
GMAF0.129
Max Magnitude
? (C;C) (C;T) (T;T) 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 22539802] Impact of MiRSNPs on survival and progression in patients with multiple myeloma undergoing autologous stem cell transplantation.


[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.