-alpha3.7 NC_000016.10:g.(172007_173726)_(175811_177537)del

HGVS Expressions

  • NC_000016.10:g.(172007_173726)_(175811_177537)del
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Clinvar 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
261550.4United Arab Emirates1Melado et al. 2024 Patient has a homozygous variant in AMH ...
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