Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569280235
rs1569280235
Entrez Id: 5456;107985635
Gene Symbol: POU3F4;LOC107985635
POU3F4;LOC107985635
CUI: C1384666
Disease:
hearing impairment
T 0.700 CausalMutation CLINVAR