NM_006005.3:c.461-9A>G

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HGVS Expressions

  • NG_011700.1:g.26339A>G
  • NM_006005.3:c.461-9A>G
  • NP_005996.2:p.?
  • NC_000004.12:g.6291188A>G

Associated Genes

Wolframin ER Transmembrane Glycoprotein
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

10010131

Clinvar

4527

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
606201.G.1Lebanon1432BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
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Contributors

  • Sami Bizzari: 11.03.2021

Edit History

  • Sami Bizzari: 14.03.2021
  • Sami Bizzari: 11.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.