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rs9966765

From SNPedia

Orientationplus
Make rs9966765(C;C)
Make rs9966765(C;G)
Make rs9966765(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome18
Position58449558
GeneLOC107985182, MIR122
is asnp
is mentioned by
dbSNPrs9966765
dbSNP (classic)rs9966765
ClinGenrs9966765
ebirs9966765
HLIrs9966765
Exacrs9966765
Gnomadrs9966765
Varsomers9966765
LitVarrs9966765
Maprs9966765
PheGenIrs9966765
Biobankrs9966765
1000 genomesrs9966765
hgdprs9966765
ensemblrs9966765
geneviewrs9966765
scholarrs9966765
googlers9966765
pharmgkbrs9966765
gwascentralrs9966765
openSNPrs9966765
23andMers9966765
SNPshotrs9966765
SNPdbers9966765
MSV3drs9966765
GWAS Ctlgrs9966765
Max Magnitude0

[PMID 30662901OA-icon.png] Single Nucleotide Polymorphisms in miR-122 Are Associated with the Risk of Hepatocellular Carcinoma in a Southern Chinese Population.