NM_019076.4:c.-41_-40dup

HGVS Expressions

  • NG_002601.2:g.32924_32925dup
  • NM_019076.4:c.-41_-40dup
  • NP_061949.3:p.?
  • NC_000002.12:g.233617667_233617668dup
Back to search Result
CTGA Clinical Significance

Pathogenic

Variant Type

Duplication

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
143500.2United Arab Emirates2PathogenicGilbert SyndromeBertoli-Avella et al. 2021
© CAGS 2024. All rights reserved.