NM_001080432.2:c.46-12906C>T

HGVS Expressions

  • NG_012969.1:g.98272C>T
  • NM_001080432.2:c.46-12906C>T
  • NP_001073901.1:p.?
  • NC_000016.10:g.53797234C>T
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Variant Type

Substitution

dbSNP

9922708

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 Emirates0.463Osman et al. 2020b 376 individuals with metabolic syndrome
605552.G.3.2United Arab Emirates0.365Osman et al. 2020b 104 control subjects
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