NG_007462.1:g.4133C>T

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HGVS Expressions

  • NG_007462.1:g.4133C>T

Associated Genes

Tumor Necrosis Factor
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Genomic Location

chr6:31574705

Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1799724

Clinvar

12389

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
614389.G.1.5Bahrain780.13BenignPregnancy Loss, Recurrent, Susceptibility to, 1Finan et al. 2010 34 heterozygotes and 10 homozygotes in a...
614389.G.1.6Bahrain1080.13BenignFinan et al. 2010 51 heterozygotes and 6 homozygotes in a ...
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Contributors

  • Pratibha Nair: 13.05.2020

Edit History

  • Pratibha Nair: 10.11.2022
  • Rahila Mir: 07.02.2022
  • Pratibha Nair: 13.05.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.