NG_007462.1:g.4127C>A

  1. Home
  2. NG_007462.1:g.4127C>A

HGVS Expressions

  • NG_007462.1:g.4127C>A

Associated Genes

Tumor Necrosis Factor
Back to search Result
Genomic Location

chr6:31574699

Clinvar Clinical Significance

Protective

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1800630

Clinvar

12390

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
614389.G.1.3Bahrain260.06BenignPregnancy Loss, Recurrent, Susceptibility to, 1Finan et al. 2010 Study of 204 patients
614389.G.1.4Bahrain650.08BenignFinan et al. 2010 31 heterozygotes and 3 homozygotes in a ...
Download Table

Contributors

  • Pratibha Nair: 13.05.2020

Edit History

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