APOE*3 Allele NM_000041.4:c.[388=;526=]

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  2. APOE*3 Allele NM_000041.4:c.[388=;526=]

HGVS Expressions

  • NG_007084.2:g.[7903=;8041=]
  • NM_000041.4:c.[388=;526=]
  • NP_000032.1:p.[Cys130=;Arg176=]
  • NC_000019.10:g.[44908684=;44908822=]

Associated Genes

Apolipoprotein E
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CTGA Clinical Significance

Risk factor, Uncertain Significance

Variant Type

Haplotype

dbSNP

429358 7412

Clinvar

17863

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
107741.G.4Lebanon3Uncertain SignificanceMahfouz et al. 2013 1 male and 2 females. The study found no...
107741.G.5Lebanon68Uncertain SignificanceMahfouz et al. 2013 15 males and 19 females. The study found...
107741.G.6Lebanon8Uncertain SignificanceMahfouz et al. 2013 5 males and 3 females. The study found n...
125853.G.10.1Lebanon957NAType 2 Diabetes MellitusAtageldiyeva et al, 2019 Group consisting of 825 T2DM patients wi...
125853.G.10.2Lebanon630NARisk factorType 2 Diabetes MellitusAtageldiyeva et al, 2019 Group consisting of 597 T2DM patients wi...
125853.G.10.3Lebanon1668NAAtageldiyeva et al, 2019 Group consisting of 1389 control subject...
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Contributors

  • Asha Deepthi: 23.11.2020

Edit History

  • Pratibha Nair: 20.06.2021
  • 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.