Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17201248
rs17201248
Entrez Id: 26797;26801;50854
Gene Symbol: SNORD52;SNORD48;SNHG32
SNORD52;SNORD48;SNHG32
CUI: C0272178
Disease:
Drug-induced neutropenia
T 0.700 GeneticVariation GWASCAT Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. 26151496 2015