NC_000023.11:g.154029098_154030767del

HGVS Expressions

  • NC_000023.11:g.154029098_154030767del
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CTGA Clinical Significance

Pathogenic

Variant Type

Deletion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
312750.16United Arab Emirates1PathogenicRett SyndromeSaleh et al. 2021 Subject had a deletion encompassing part...
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