NC_000002.12:g.203876827G>A

HGVS Expressions

  • NC_000002.12:g.203876827G>A
  • NC_000002.12:g.203876827G>A
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

231727

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 Emirates730.263BenignSharma et al. 2021 139 patients with Type I diabetes. Signi...
222100.G.5.2United Arab Emirates690.202BenignSharma et al. 2021 171 healthy controls
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