NM_000527.4:c.940+36G>A

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HGVS Expressions

  • NG_009060.1:g.23170G>A
  • NM_000527.4:c.940+36G>A
  • NP_000518.1:p.?
  • NC_000019.10:g.11107550G>A

Associated Genes

Low Density Lipoprotein Receptor
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

13306513

Clinvar

523739

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
606945.GUnited Arab Emirates60.075BenignMazrooei & Mohamed 2010 11 benign polymorphisms identified in a ...
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Contributors

  • Sami Bizzari: 10.03.2022

Edit History

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