NM_020820.3:c.1036+412=

HGVS Expressions

  • NM_020820.3:c.1036+412=
  • NP_065871.2:p.?
  • NC_000020.11:g.48692260=
Back to search Result
Variant Type

Reference Allele

dbSNP

6095241

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605552.G.3.1United Arab Emirates0.372Osman et al. 2020b 376 individuals with metabolic syndrome
605552.G.3.2United Arab Emirates0.466Osman et al. 2020b 104 control subjects
© CAGS 2024. All rights reserved.