NM_000401.3:c.2035-41T>C

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HGVS Expressions

  • NG_007560.1:g.145704T>C
  • NM_000401.3:c.2035-41T>C
  • NC_000011.10:g.44236252T>C

Associated Genes

Exostosin Glycosyltransferase 2
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

3740878

Clinvar

263290

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.19.1Lebanon4030.203BenignType 2 Diabetes MellitusNemr et al. 2013 995 diabetic patients
125853.G.19.2Lebanon3710.172BenignNemr et al. 2013 1076 control subjects
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Contributors

  • Pratibha Nair: 16.03.2021

Edit History

  • Pratibha Nair: 16.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.