NM_001850.4:c.-4+13317C=

HGVS Expressions

  • NM_001850.4:c.-4+13317C=
  • NP_001841.2:p.?
  • NC_000003.12:g.99758338C=
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CTGA Clinical Significance

Association

Variant Type

Reference Allele

dbSNP

792837

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.15.1Lebanon907AssociationType 2 Diabetes MellitusAlmawi et al. 2013 Study with 995 T2DM patients. 907/1083 a...
125853.G.15.2Lebanon877AssociationAlmawi et al. 2013 Study with 1076 controls. 877/1513 allel...
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