ESPN, espin, 83715

N. diseases: 28; N. variants: 7
Disease: hearing impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs754472294
rs754472294
Entrez Id: 83715
Gene Symbol: ESPN
ESPN
CUI: C1384666
Disease:
hearing impairment 		A 0.700 CausalMutation CLINVAR