NR_003529.3:n.2908+1228A>G

HGVS Expressions

  • NR_003529.3:n.2908+1228A>G
  • NC_000009.12:g.22115027A>G

Associated Genes

CDKN2B Antisense RNA
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CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

2383206

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 Emirates4380.64Likely BenignType 2 Diabetes MellitusBaalfaqih et al. 2020 341 T2DM patients without coronary arter...
125853.G.34.2United Arab Emirates2350.66Likely BenignType 2 Diabetes MellitusBaalfaqih et al. 2020 178 T2DM patients with coronary artery d...
125853.G.34.3United Arab Emirates5780.64Baalfaqih et al. 2020 Group consisting of 450 control subjects...
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