276902.G.2

Country

United Arab Emirates

HPO Terms

Congenital sensorineural hearing impairment

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NC_000003.12:g.150649557_15065992inv4

Remarks

Two individuals harboring a large inversion in exon 2 of CLRN1
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