NM_207362.2:c.70+169C>A

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HGVS Expressions

  • NM_207362.2:c.70+169C>A
  • NP_997245.2:p.?
  • NC_000002.12:g.98846562G>T

Associated Genes

CRACDL Gene
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

12712037

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
610064.G.1United Arab EmiratesAssociationOpioid Dependence, Susceptibility to, 1Alblooshi et al. 2020 250 Emirati patients
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Contributors

  • Pratibha Nair: 17.05.2022

Edit History

  • Pratibha Nair: 05.12.2022
  • Pratibha Nair: 17.05.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.