NM_001350748.2:c.1764+21dup

HGVS Expressions

  • NG_053176.1:g.230311dup
  • NM_001350748.2:c.1764+21dup
Back to search Result
Genomic Location

chr13:101191904

CTGA Clinical Significance

Benign

Variant Type

Duplication

dbSNP

5806198

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615419.13Morocco1BenignBramswig et al. 2018
© CAGS 2024. All rights reserved.