NM_003761.4:c.*143T>C

HGVS Expressions

  • NG_022887.1:g.9369T>C
  • NM_003761.4:c.*143T>C
  • NP_003752.2:p.?
  • NC_000002.12:g.85581859T>C
Back to search Result
Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

1010

Clinvar

1182311

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608320.G.2.3United Arab EmiratesNAAssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
© CAGS 2024. All rights reserved.