NM_001311311.1:c.-1639G>T

HGVS Expressions

  • NG_011564.1:g.3588G>T
  • NM_001311311.1:c.-1639G>T
Back to search Result
Genomic Location

chr16:31096368

Clinvar Clinical Significance

Drug Response

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

9923231

Clinvar

226030

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608547.G.1Lebanon0.524Drug ResponseOssaily and Zgheib. 2014
© CAGS 2024. All rights reserved.