NC_000010.10:g.23508437A>G

HGVS Expressions

  • NC_000010.10:g.23508437A>G
  • NC_000010.10:g.23508437A>G
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CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615935.1.1Syria2PathogenicPancreatic Agenesis 2Weedon et al. 2014
615935.1.2Syria2PathogenicPancreatic Agenesis 2Weedon et al. 2014 Sibling of 615935.1
615935.1.3Syria2PathogenicPancreatic Agenesis 2Weedon et al. 2014 Sibling of 615935.1.1
615935.2Lebanon2PathogenicPancreatic Agenesis 2Weedon et al. 2014
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