NM_000527.4:c.*52G>A

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  2. NM_000527.4:c.*52G>A

HGVS Expressions

  • NG_009060.1:g.46988G>A
  • NM_000527.4:c.*52G>A
  • NP_000518.1:p.?
  • NC_000019.10:g.11131368G>A

Associated Genes

Low Density Lipoprotein Receptor
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

14158

Clinvar

265910

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
606945.GUnited Arab Emirates130.163BenignMazrooei & Mohamed 2010 11 benign polymorphisms identified in a ...
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Contributors

  • Sami Bizzari: 10.03.2022

Edit History

  • Sami Bizzari: 11.03.2022
  • Sami Bizzari: 10.03.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.