OTOA, otoancorin, 146183

N. diseases: 12; N. variants: 7
Disease: Deafness, Autosomal Recessive 22 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1567396832
rs1567396832
Entrez Id: 146183
Gene Symbol: OTOA
OTOA
CUI: C1846896
Disease:
Deafness, Autosomal Recessive 22 		T 0.700 GeneticVariation CLINVAR Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees. 30828794 2019