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rs2289030

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2289030(C;G)
Make rs2289030(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position94834510
GeneKRT19P2, MIR492
is asnp
is mentioned by
dbSNPrs2289030
ebirs2289030
HLIrs2289030
Exacrs2289030
Varsomers2289030
Maprs2289030
PheGenIrs2289030
hapmaprs2289030
1000 genomesrs2289030
hgdprs2289030
ensemblrs2289030
gopubmedrs2289030
geneviewrs2289030
scholarrs2289030
googlers2289030
pharmgkbrs2289030
gwascentralrs2289030
openSNPrs2289030
23andMers2289030
23andMe allrs2289030
SNP Nexus

SNPshotrs2289030
SNPdbers2289030
MSV3drs2289030
GWAS Ctlgrs2289030
GMAF0.118
Max Magnitude0
? (C;C) (C;G) (G;G) 28

[PMID 20044760] Prognostic impact of microRNA-related gene polymorphisms on survival of patients with colorectal cancer


[PMID 19047128OA-icon.png] Single nucleotide polymorphisms of microRNA machinery genes modify the risk of renal cell carcinoma.


[PMID 19138993OA-icon.png] Genetic variations in microRNA-related genes are novel susceptibility loci for esophageal cancer risk.


[PMID 19232555OA-icon.png] Signatures of purifying and local positive selection in human miRNAs.


[PMID 19458495OA-icon.png] Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.


[PMID 22818121] The prognostic impact of microRNA sequence polymorphisms on the recurrence of patients with completely resected non-small cell lung cancer


[PMID 26753964] miR-492G>C polymorphism (rs2289030) is associated with overall survival of hepatocellular carcinoma patients.