NM_024408.4:c.875-5592C>A

HGVS Expressions

  • NG_008163.1:g.99318C>A
  • NM_024408.4:c.875-5592C>A
  • NP_077719.2:p.?
  • NC_000001.11:g.119975336G>T

Associated Genes

NOTCH2 N-Terminal-Like R
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CTGA Clinical Significance

Benign

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605734.G.1Lebanon382BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
611800.G.1Lebanon312BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
618026.G.1Lebanon301BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
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