NM_001365276.2:c.11381-?_11524+?del

HGVS Expressions

  • NM_001365276.2:c.11381-?_11524+?del

Associated Genes

Tenascin XB
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Variant Type

Deletion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyClinical SignificanceCondition(s)ReferenceRemarks
131100.2United Arab Emirates2Likely PathogenicEhlers-Danlos Syndrome, Classic-LikeChen Cardenas et al. 2020
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