NM_182492.2:c.439-38_439-37insGCCATT

HGVS Expressions

  • NM_182492.2:c.439-38_439-37insGCCATT
  • NC_000022.11:g.25354852_25354853insAATGGC
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Variant Type

Insertion

dbSNP

16388

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605977.G.1United Arab Emirates0.474Almheiri et al. 2019 500 healthy Emiratis (254 females)
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