NM_003235.4:c.3433+3_3433+6del

HGVS Expressions

  • NG_015832.1:g.38383_38386del
  • NM_003235.4:c.3433+3_3433+6del
  • NC_000008.11:g.132900342_132900345del

Associated Genes

Thyroglobulin
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Deletion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
274700.4.1Somalia1Uncertain SignificanceThyroid Dyshormonogenesis 3Nicholas et al. 2016 The authors noted that the genotype asce...
274700.4.2Somalia1Uncertain SignificanceThyroid Dyshormonogenesis 3Nicholas et al. 2016 Brother of 274700.4.1
274700.4.3Somalia1Uncertain SignificanceThyroid Dyshormonogenesis 3Nicholas et al. 2016 Brother of 274700.4.1
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