NM_000305.2:c.146-1542_146-1541insTGTGTAGGCAT

HGVS Expressions

  • NM_000305.2:c.146-1542_146-1541insTGTGTAGGCAT
  • NP_000296.2:p.?
  • NC_000007.13:g.95047153_95047154insATGCCTACACA

Associated Genes

Paraoxonase 2
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Variant Type

Insertion

dbSNP

3831551

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605977.G.1United Arab Emirates0.478Almheiri et al. 2019 500 healthy Emiratis (254 females)
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