NC_000011.10:g.76917135_76917255

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HGVS Expressions

  • NC_000011.10:g.76917135_76917255
  • NC_000011.10:g.76917135_76917255

Associated Genes

Myosin VIIA
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Clinvar Clinical Significance

Likely Pathogenic

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Deletion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
600060.G.2United Arab Emirates4Likely PathogenicDeafness, Autosomal Recessive 2Elsayed O and Al-Shamsi A. 2022 Two patients with deafness exhibiting a ...
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Contributors

  • Sami Bizzari: 16.11.2023

Edit History

  • Sami Bizzari: 16.11.2023
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.