MIR22, microRNA 22, 407004

N. diseases: 195; N. variants: 2
Disease: Serum albumin measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11078597
rs11078597
Entrez Id: 84981;124997;407004
Gene Symbol: MIR22HG;WDR81;MIR22
MIR22HG;WDR81;MIR22
CUI: C0523465
Disease:
Serum albumin measurement 		C 0.800 GeneticVariation GWASCAT Discovery and fine mapping of serum protein loci through transethnic meta-analysis. 23022100 2012
dbSNP: rs11078597
rs11078597
Entrez Id: 84981;124997;407004
Gene Symbol: MIR22HG;WDR81;MIR22
MIR22HG;WDR81;MIR22
CUI: C0523465
Disease:
Serum albumin measurement 		C 0.800 GeneticVariation GWASDB Discovery and fine mapping of serum protein loci through transethnic meta-analysis. 23022100 2012