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rs213210

From SNPedia

Orientationminus
Stabilizedminus
Make rs213210(C;C)
Make rs213210(C;T)
Make rs213210(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position33208047
GeneMIR219A1, RING1
is asnp
is mentioned by
dbSNPrs213210
dbSNP (classic)rs213210
ClinGenrs213210
ebirs213210
HLIrs213210
Exacrs213210
Gnomadrs213210
Varsomers213210
LitVarrs213210
Maprs213210
PheGenIrs213210
Biobankrs213210
1000 genomesrs213210
hgdprs213210
ensemblrs213210
geneviewrs213210
scholarrs213210
googlers213210
pharmgkbrs213210
gwascentralrs213210
openSNPrs213210
23andMers213210
SNPshotrs213210
SNPdbers213210
MSV3drs213210
GWAS Ctlgrs213210
GMAF0.191
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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


[PMID 23508906] Association of polymorphism in MicroRNA 219-1 with clearance of hepatitis B virus infection


[PMID 24205249OA-icon.png] MicroRNA Polymorphisms and Environmental Smoke Exposure as Risk Factors for Oesophageal Squamous Cell Carcinoma


[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 22661538OA-icon.png] Genetic polymorphisms in MicroRNA-related genes as predictors of clinical outcomes in colorectal adenocarcinoma patients.


[PMID 26379361OA-icon.png] A Genetic Variant in miRNA-219-1 Is Associated with Risk of Esophageal Squamous Cell Carcinoma in Chinese Kazakhs


[PMID 28455989] Polymorphisms of pri-miR-219-1 are associated with the susceptibility and prognosis of non-small cell lung cancer in a Northeast Chinese population.


[PMID 28915609OA-icon.png] Polymorphisms of pri-miR-219-1 are associated with the susceptibility and prognosis of non-small cell lung cancer in a Northeast Chinese population.


[PMID 31551439OA-icon.png] Association between single nucleotide polymorphisms within HLA region and disease relapse for patients with hematopoietic stem cell transplantation.