Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1559320299
rs1559320299
Entrez Id: 5077;151278
Gene Symbol: PAX3;CCDC140
PAX3;CCDC140
CUI: C0018784
Disease:
Sensorineural Hearing Loss (disorder)
A 0.700 GeneticVariation CLINVAR