600974.1.6

Country

Algeria

HPO Terms

Hearing impairment

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_138691.2:c.100C>T2

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
600974.1.1AlgeriaHearing impairmentUnknown
600974.1.2AlgeriaHearing impairmentUnknown
600974.1.3AlgeriaHearing impairmentUnknown
600974.1.4AlgeriaHearing impairmentUnknown
600974.1.5AlgeriaHearing impairmentUnknown
600974.1.7AlgeriaHearing impairmentUnknown
600974.1.8AlgeriaHearing impairmentUnknown
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