NC_000016.10:g.56959412C>A

HGVS Expressions

  • NG_008952.1:g.2490C>A
  • NC_000016.10:g.56959412C>A
  • NC_000016.10:g.56959412C>A
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

3764261

Clinvar

162176

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
143470.G.1LebanonAssociationDeek et al. 2019 Study with 2700 subjects. Significant as...
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