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

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

Epidemiology in the Arab World

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Subject ID	Country of Origin	Allele Count	Allele Frequency	CTGA Clinical Significance	Condition(s)	Reference	Remarks
107741.1	Lebanon	1		Uncertain Significance		Mahfouz et al. 2013	The study found no associations.
107741.G.4	Lebanon	3		Uncertain Significance		Mahfouz et al. 2013	1 male and 2 females. The study found no...
125853.G.10.1	Lebanon	186	NA		Type 2 Diabetes Mellitus	Atageldiyeva et al, 2019	Group consisting of 825 T2DM patients wi...
125853.G.10.2	Lebanon	217	NA	Risk factor	Type 2 Diabetes Mellitus	Atageldiyeva et al, 2019	Group consisting of 597 T2DM patients wi...
125853.G.10.3	Lebanon	550	NA			Atageldiyeva 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 2025. All rights reserved.