NM_001370259.2:c.784-9G>A

HGVS Expressions

  • NG_008929.1:g.9067G>A
  • NM_001370259.2:c.784-9G>A
  • NC_000011.10:g.64807228C>T

Associated Genes

Menin 1
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Clinical Significance

Likely Pathogenic,Pathogenic

Variant Type

Substitution

Clinvar

200981

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyClinical SignificanceCondition(s)ReferenceRemarks
131100.2United Arab Emirates1Likely PathogenicMultiple Endocrine Neoplasia, Type IChen Cardenas et al. 2020
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