NOP58, NOP58 ribonucleoprotein, 51602

N. diseases: 3; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4470328
rs4470328
Entrez Id: 51602
Gene Symbol: NOP58
NOP58
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019