NM_001040021.3:c.-121-139T>C

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HGVS Expressions

  • NG_023178.1:g.5371T>C
  • NM_001040021.3:c.-121-139T>C

Associated Genes

Monocyte Differentiation Antigen CD14
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Genomic Location

chr5:140633331

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

2569190

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
143890.G.3LebanonNAAssociationSalami et al, 2019 Study indicated association of G allele ...
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Contributors

  • Asha Deepthi: 11.11.2020

Edit History

  • Asha Deepthi: 11.11.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.