NM_000218.2:c.1795-29246C>T

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HGVS Expressions

  • NG_008935.1:g.378531C>T
  • NM_000218.2:c.1795-29246C>T
  • NP_000209.2:p.?
  • NC_000011.10:g.2818521C>T

Associated Genes

Potassium Channel, Voltage-Gated, KQT-Like Subfamily, Member 1
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CTGA Clinical Significance

Association, Benign

Variant Type

Substitution

dbSNP

2237892

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.16.1Lebanon620AssociationType 2 Diabetes MellitusAlmawi et al. 2013 Study with 995 T2DM patients. 620/1370 a...
125853.G.16.2Lebanon363BenignAlmawi et al. 2013 Study with 1076 controls. 363/2027 allel...
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Contributors

  • Sami Bizzari: 11.03.2021

Edit History

  • Rahila Mir: 22.02.2022
  • Sami Bizzari: 14.03.2021
  • Sami Bizzari: 11.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.