NM_006548.6:c.239+29254C>A

HGVS Expressions

  • NG_011602.1:g.36141C>A
  • NM_006548.6:c.239+29254C>A
Back to search Result
Genomic Location

chr3:185793899

Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

4402960

Clinvar

2435

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.5.1Lebanon3960.37AssociationType 2 Diabetes MellitusNemr et al, 2012b Study with 544 T2DM patients
125853.G.5.2Lebanon3240.27Nemr et al, 2012b Group consisting of 606 control subjects
© CAGS 2024. All rights reserved.