NM_001351.4:c.571-1G>C

HGVS Expressions

  • NG_023329.1:g.15916G>C
  • NM_001351.4:c.571-1G>C
  • NC_000003.12:g.16594584C>G
Back to search Result
CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
258150.6Saudi Arabia2Likely PathogenicSpermatogenic Failure 1Alhathal et al. 2020
© CAGS 2024. All rights reserved.