NM_207362.2:c.-10-3458C>T

HGVS Expressions

  • NM_207362.2:c.-10-3458C>T
  • NP_997245.2:p.?
  • NC_000002.12:g.98850268G>A

Associated Genes

CRACDL Gene
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CTGA Clinical Significance

Association

Variant Type

Substitution

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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