rs9966765
From SNPedia
Orientation | plus |
Make rs9966765(C;C) |
Make rs9966765(C;G) |
Make rs9966765(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 18 |
Position | 58449558 |
Gene | LOC107985182, MIR122 |
is a | snp |
is | mentioned by |
dbSNP | rs9966765 |
dbSNP (classic) | rs9966765 |
ClinGen | rs9966765 |
ebi | rs9966765 |
HLI | rs9966765 |
Exac | rs9966765 |
Gnomad | rs9966765 |
Varsome | rs9966765 |
LitVar | rs9966765 |
Map | rs9966765 |
PheGenI | rs9966765 |
Biobank | rs9966765 |
1000 genomes | rs9966765 |
hgdp | rs9966765 |
ensembl | rs9966765 |
geneview | rs9966765 |
scholar | rs9966765 |
rs9966765 | |
pharmgkb | rs9966765 |
gwascentral | rs9966765 |
openSNP | rs9966765 |
23andMe | rs9966765 |
SNPshot | rs9966765 |
SNPdbe | rs9966765 |
MSV3d | rs9966765 |
GWAS Ctlg | rs9966765 |
Max Magnitude | 0 |
[PMID 30662901] Single Nucleotide Polymorphisms in miR-122 Are Associated with the Risk of Hepatocellular Carcinoma in a Southern Chinese Population.