NM_000777.4:c.219-237G=

HGVS Expressions

  • NG_007938.1:g.12083G>A
  • NM_000777.4:c.219-237G=
  • NC_000007.14:g.99672916T>C
Back to search Result
Clinvar Clinical Significance

Drug Response

Variant Type

Reference Allele

dbSNP

776746

Clinvar

226021

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
256700.G.1Lebanon47Darwish et al. 2015 27 children diagnosed with neuroblastoma...
© CAGS 2024. All rights reserved.