Disease: hearing impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554581757
rs1554581757
Entrez Id: 55636
Gene Symbol: CHD7
CHD7
CUI: C1384666
Disease:
hearing impairment 		T 0.700 CausalMutation CLINVAR