NG_007462.1:g.4614G>A

  1. Home
  2. NG_007462.1:g.4614G>A

HGVS Expressions

  • NG_007462.1:g.4614G>A

Associated Genes

Tumor Necrosis Factor
Back to search Result
Genomic Location

chr6:31575186

Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Risk factor

Variant Type

Substitution

dbSNP

1800750

Clinvar

12387

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
614389.G.1.7Bahrain500.1Risk factorPregnancy Loss, Recurrent, Susceptibility to, 1Finan et al. 2010 20 heterozygotes and 10 homozygotes in a...
614389.G.1.8Bahrain220.04Risk factorFinan et al. 2010 Study of 248 controls
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.