NM_001242648.2:c.251-149640A>C

HGVS Expressions

  • NM_001242648.2:c.251-149640A>C
  • NP_001229577.1:p.?
  • NC_000006.12:g.12903725A>C
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CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

9349379

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608320.G.1LebanonAssociationCoronary Artery Disease, Autosomal Dominant, 1Hager et al. 2012 Study on 1949 patients with coronary art...
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