NM_000401.3:c.1906-51T>C

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HGVS Expressions

  • NG_007560.1:g.143516T>C
  • NM_000401.3:c.1906-51T>C
  • NP_000392.3:p.?
  • NC_000011.10:g.44234064T>C

Associated Genes

Exostosin Glycosyltransferase 2
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

11037909

Clinvar

1166104

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.19.1Lebanon4320.217BenignType 2 Diabetes MellitusNemr et al. 2013 995 diabetic patients
125853.G.19.2Lebanon3920.182BenignNemr et al. 2013 1076 control subjects
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Contributors

  • Pratibha Nair: 16.03.2021

Edit History

  • Pratibha Nair: 21.11.2022
  • Rahila Mir: 07.02.2022
  • Pratibha Nair: 16.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.