NC_000015.10:g.22765628_28691460del

HGVS Expressions

  • NC_000015.10:g.22765628_28691460del
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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
176270.1United Arab Emirates1Likely PathogenicPrader-Willi SyndromeAlabdullatif et al. 2017
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