rs112489955
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs112489955(A;A) |
Make rs112489955(A;G) |
Make rs112489955(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 50009781 |
Gene | CLCN5, MIR500B, MIR501 |
is a | snp |
is | mentioned by |
dbSNP | rs112489955 |
dbSNP (classic) | rs112489955 |
ClinGen | rs112489955 |
ebi | rs112489955 |
HLI | rs112489955 |
Exac | rs112489955 |
Gnomad | rs112489955 |
Varsome | rs112489955 |
LitVar | rs112489955 |
Map | rs112489955 |
PheGenI | rs112489955 |
Biobank | rs112489955 |
1000 genomes | rs112489955 |
hgdp | rs112489955 |
ensembl | rs112489955 |
geneview | rs112489955 |
scholar | rs112489955 |
rs112489955 | |
pharmgkb | rs112489955 |
gwascentral | rs112489955 |
openSNP | rs112489955 |
23andMe | rs112489955 |
SNPshot | rs112489955 |
SNPdbe | rs112489955 |
MSV3d | rs112489955 |
GWAS Ctlg | rs112489955 |
Max Magnitude | 0 |
[PMID 27310251] A Function Variant at miR-501 Alters Susceptibility to Hepatocellular Carcinoma in a Chinese Han Population.