Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4280164
rs4280164
Entrez Id: 161424
Gene Symbol: NOP9
NOP9
CUI: C3809483
Disease:
SPECIFIC LANGUAGE IMPAIRMENT 5
G 0.700 GeneticVariation GWASCAT Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. 24571439 2014