NM_001709.5:c.*2327=

HGVS Expressions

  • NG_011794.1:g.71564A>G
  • NM_001709.5:c.*2327=
  • NP_001700.2:p.?
  • NC_000011.10:g.27655494=
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Variant Type

Reference Allele

dbSNP

7124442

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605552.G.3.1United Arab Emirates0.313Osman et al. 2020b 376 individuals with metabolic syndrome
605552.G.3.2United Arab Emirates0.236Osman et al. 2020b 104 control subjects
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