NM_175061.3:c.115+39526A>T

HGVS Expressions

  • NG_011499.1:g.44882A>T
  • NM_175061.3:c.115+39526A>T
  • NP_778231.2:p.?
  • NC_000007.14:g.28140937T>A

Associated Genes

JAZF Zinc Finger 1
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

864745

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
606246.G.1Lebanon1967BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
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