NC_000009.12:g.22125504G>C

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HGVS Expressions

  • NC_000009.12:g.22125504G>C
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Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

1333049

Clinvar

812642

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.34.1United Arab Emirates3130.46Likely BenignType 2 Diabetes MellitusBaalfaqih et al. 2020 341 T2DM patients without coronary arter...
125853.G.34.2United Arab Emirates1680.47Likely BenignType 2 Diabetes MellitusBaalfaqih et al. 2020 178 T2DM patients with coronary artery d...
125853.G.34.3United Arab Emirates4000.44Baalfaqih et al. 2020 Group consisting of 450 control subjects...
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Contributors

  • Asha Deepthi: 18.03.2022

Edit History

  • Asha Deepthi: 21.03.2022
  • Asha Deepthi: 18.03.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.