NM_000184.2:c.-211C>T

  1. Home
  2. NM_000184.2:c.-211C>T

HGVS Expressions

  • NG_000007.3:g.42677C>T
  • NM_000184.2:c.-211C>T

Associated Genes

Hemoglobin, Gamma G
Back to search Result
Genomic Location

chr11:5254939

Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

7482144

Clinvar

14984

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
141749.G.1.1Saudi Arabia26Uncertain SignificanceFetal Hemoglobin Quantitative Trait Locus 1Miller et al. 1987 13 patients with sickle cell anemia
141749.G.1.2Saudi Arabia3Uncertain SignificanceFetal Hemoglobin Quantitative Trait Locus 1Miller et al. 1987 3 patients with sickle cell anemia
141749.G.1.3Saudi Arabia8Uncertain SignificanceFetal Hemoglobin Quantitative Trait Locus 1Miller et al. 1987 4 individuals with sickle cell trait
141749.G.1.4Saudi Arabia9Uncertain SignificanceFetal Hemoglobin Quantitative Trait Locus 1Miller et al. 1987 9 individuals with sickle cell trait
Download Table

Contributors

  • Sayeeda Hana: 22.11.2020

Edit History

  • Sayeeda Hana: 25.03.2021
  • Sayeeda Hana: 23.11.2020
  • Sayeeda Hana: 22.11.2020
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.