NM_000527.4:c.-120C>T

HGVS Expressions

  • NG_009060.1:g.5049C>T
  • NM_000527.4:c.-120C>T
  • NP_000518.1:p.?
  • NC_000019.10:g.11089429C>T
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Clinvar Clinical Significance

Likely Benign, Likely Pathogenic, Uncertain Significance

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Clinvar

226299

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
143890.67United Arab Emirates1NALikely PathogenicHypercholesterolemia, Familial, 1Rimbert et al. 2021 'Patient 813' in the publication
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