OTOGL, otogelin like, 283310

N. diseases: 9; N. variants: 8
Disease: hearing impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1477766714
rs1477766714
Entrez Id: 283310
Gene Symbol: OTOGL
OTOGL
CUI: C1384666
Disease:
hearing impairment 		G 0.700 GeneticVariation CLINVAR