NM_001319217.2:c.*595T>G

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  2. NM_001319217.2:c.*595T>G

HGVS Expressions

  • NG_061374.1:g.10635T>G
  • NM_001319217.2:c.*595T>G
  • NC_000015.10:g.74719894A>C

Associated Genes

Cytochrome P450, Subfamily I, Polypeptide 1
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1800031

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
108330.G.2Arab.010BenignMartínez-Labarga et al. 2019 58 healthy Arabs from Dubai, UAE
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Contributors

  • Pratibha Nair: 10.03.2022

Edit History

  • Pratibha Nair: 10.03.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.