NC_000001.11:g.55030366T>A

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HGVS Expressions

  • NC_000001.11:g.55030366T>A

Associated Genes

Proprotein Convertase, Subtilisin/Kexin-Type, 9
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

11206510

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608446.G.1LebanonBenignSaade et al. 2011 Study of 2002 Lebanese subjects to asses...
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Contributors

  • Sayeeda Hana: 24.03.2021

Edit History

  • Rahila Mir: 22.02.2022
  • Sayeeda Hana: 29.03.2021
  • Sayeeda Hana: 24.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.