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rs112489955

From SNPedia

Orientationplus
Stabilizedplus
Make rs112489955(A;A)
Make rs112489955(A;G)
Make rs112489955(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position50009781
GeneCLCN5, MIR500B, MIR501
is asnp
is mentioned by
dbSNPrs112489955
dbSNP (old)rs112489955
ClinGenrs112489955
ebirs112489955
HLIrs112489955
Exacrs112489955
Gnomadrs112489955
Varsomers112489955
Maprs112489955
PheGenIrs112489955
Biobankrs112489955
1000 genomesrs112489955
hgdprs112489955
ensemblrs112489955
gopubmedrs112489955
geneviewrs112489955
scholarrs112489955
googlers112489955
pharmgkbrs112489955
gwascentralrs112489955
openSNPrs112489955
23andMers112489955
23andMe allrs112489955
SNP Nexus

SNPshotrs112489955
SNPdbers112489955
MSV3drs112489955
GWAS Ctlgrs112489955
Max Magnitude

[PMID 27310251] A Function Variant at miR-501 Alters Susceptibility to Hepatocellular Carcinoma in a Chinese Han Population.