Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1558939623
rs1558939623
Entrez Id: 1123
Gene Symbol: CHN1
CHN1
CUI: C0018784
Disease:
Sensorineural Hearing Loss (disorder)
T 0.700 GeneticVariation CLINVAR