NM_001350748.2:c.4042-50CT[5]

HGVS Expressions

  • NG_053176.1:g.347495_347496CT[5]
  • NM_001350748.2:c.4042-50CT[5]
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Genomic Location

chr13:101074694-101074695

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Duplication

Clinvar

802996

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615419.13Morocco1BenignBramswig et al. 2018
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