APOE*2 Allele NM_000041.4:c.[388=;526C>T]

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  2. APOE*2 Allele NM_000041.4:c.[388=;526C>T]

HGVS Expressions

  • NG_007084.2:g.[7903=;8041C>T]
  • NM_000041.4:c.[388=;526C>T]
  • NP_000032.1:p.[Cys130=;Arg176Cys]
  • NC_000019.10:g.[44908684=;44908822C>T]

Associated Genes

Apolipoprotein E
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CTGA Clinical Significance

Risk factor, Uncertain Significance

Variant Type

Haplotype

dbSNP

429358 7412

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
107741.1Lebanon1Uncertain SignificanceMahfouz et al. 2013 The study found no associations.
107741.G.4Lebanon3Uncertain SignificanceMahfouz et al. 2013 1 male and 2 females. The study found no...
125853.G.10.1Lebanon186NAType 2 Diabetes MellitusAtageldiyeva et al, 2019 Group consisting of 825 T2DM patients wi...
125853.G.10.2Lebanon217NARisk factorType 2 Diabetes MellitusAtageldiyeva et al, 2019 Group consisting of 597 T2DM patients wi...
125853.G.10.3Lebanon550NAAtageldiyeva et al, 2019 Group consisting of 1389 control subject...
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Contributors

  • Asha Deepthi: 23.11.2020

Edit History

  • Asha Deepthi: 31.05.2021
  • Sami Bizzari: 16.03.2021
  • Asha Deepthi: 18.01.2021
  • Asha Deepthi: 17.12.2020
  • Asha Deepthi: 13.12.2020
  • Asha Deepthi: 23.11.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.