NM_000525.3:c.67A>G

HGVS Expressions

  • NG_012446.1:g.5635A>G
  • NM_000525.3:c.67A>G
  • NP_000516.3:p.Lys23Glu
  • NC_000011.10:g.17388025T>C
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Clinvar Clinical Significance

Benign, Likely Benign, Risk factor

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

5219

Clinvar

8678

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.6.1Lebanon0.279Type 2 Diabetes MellitusMtiraoui et al, 2012 Study with 751 Lebanese T2DM patients
125853.G.6.2Lebanon0.266Mtiraoui et al, 2012 Group consisting of 918 Lebanese control...
125853.G.6.3Tunisia0.329AssociationType 2 Diabetes MellitusMtiraoui et al, 2012 Study with 1470 Tunisian T2DM patients
125853.G.6.4Tunisia0.279AssociationMtiraoui et al, 2012 Group consisting of 838 Tunisian control...
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