NC_000002.12:g.203874196G>A

HGVS Expressions

  • NG_011502.1:g.11411G>A
  • NC_000002.12:g.203874196G>A
  • NC_000002.12:g.203874196G>A
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

3087243

Clinvar

16922

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
222100.G.5.1United Arab Emirates1300.468BenignSharma et al. 2021 139 patients with Type I diabetes. Signi...
222100.G.5.2United Arab Emirates1890.553BenignSharma et al. 2021 171 healthy controls
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