NM_000218.2:c.1795-11803A>C

HGVS Expressions

  • NG_008935.1:g.395974A>C
  • NM_000218.2:c.1795-11803A>C
  • NP_000209.2:p.?
  • NC_000011.10:g.2835964A>C
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

2237895

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.16.3Lebanon849AssociationType 2 Diabetes MellitusAlmawi et al. 2013 Study with 995 T2DM patients. 849/1141 a...
125853.G.16.4Lebanon917AssociationAlmawi et al. 2013 Study with 1076 controls. 917/1473 allel...
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