NC_000004.12:g.46174811G>A

HGVS Expressions

  • NC_000004.12:g.46174811G>A
Back to search Result
CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

7662743

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.35.1United Arab EmiratesNANAAssociationType 2 Diabetes MellitusAl Safar et al. 2013 Discovery GWAS group comprising 178 indi...
© CAGS 2024. All rights reserved.