NM_000594.3:c.-488G>A - CAGS

NM_000594.3:c.-488G>A

HGVS Expressions

NG_007462.1:g.4682G>A
NM_000594.3:c.-488G>A
NC_000006.12:g.31575254G>A

Associated Genes

Tumor Necrosis Factor

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Clinvar Clinical Significance

Drug Response

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

Clinvar

Epidemiology in the Arab World

Subject ID	Country of Origin	Allele Count	Allele Frequency	CTGA Clinical Significance	Condition(s)	Reference	Remarks
Lebanese Cytokine	Lebanon		0.0755	Benign		Mahfouz et al. 2009	Frequency of cytokine gene alleles in 10...
145500.G.10.1	United Arab Emirates	25	0.15	Benign		Frossard et al. 2002	70 hypertensives
145500.G.10.2	United Arab Emirates	37	0.2	Benign		Frossard et al. 2002	72 normotensives
614389.G.1.9	Bahrain	72	0.12	Benign	Pregnancy Loss, Recurrent, Susceptibility to, 1	Finan et al. 2010	32 heterozygotes and 8 homozygotes in a ...
614389.G.1.10	Bahrain	68	0.08	Benign		Finan et al. 2010	32 heterozygotes and 4 homozygotes in a ...

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Contributors

Pratibha Nair: 05.09.2021
Pratibha Nair: 13.05.2020

Edit History

Sayeeda Hana: 13.01.2023
Pratibha Nair: 05.09.2021
Sami Bizzari: 01.06.2021
Sami Bizzari: 29.03.2021
Pratibha Nair: 13.05.2020

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© CAGS 2024. All rights reserved.

© CAGS 2024. All rights reserved.