NR_003529.3:n.2698+1211A>G

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HGVS Expressions

  • NR_003529.3:n.2698+1211A>G
  • NC_000009.12:g.22098575A>G

Associated Genes

CDKN2B Antisense RNA
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Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Association, Likely Benign

Variant Type

Substitution

dbSNP

4977574

Clinvar

812644

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 Emirates3950.58Likely BenignType 2 Diabetes MellitusBaalfaqih et al. 2020 341 T2DM patients without coronary arter...
125853.G.34.2United Arab Emirates1930.54Likely BenignType 2 Diabetes MellitusBaalfaqih et al. 2020 178 T2DM patients with coronary artery d...
125853.G.34.3United Arab Emirates4840.54Baalfaqih et al. 2020 Group consisting of 450 control subjects...
608446.G.1LebanonAssociationMyocardial Infarction, Susceptibility to, 1Saade et al. 2011 Study of 2002 Lebanese subjects to asses...
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Contributors

  • Sayeeda Hana: 23.03.2021

Edit History

  • Asha Deepthi: 21.03.2022
  • Sayeeda Hana: 29.03.2021
  • Sayeeda Hana: 23.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.