NM_000059.3:c.-26G>A

HGVS Expressions

  • NG_012772.3:g.5956G>A
  • NM_000059.3:c.-26G>A

Associated Genes

BRCA2 Gene
Back to search Result
Genomic Location

chr13:32316435

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1799943

Clinvar

125965

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.41LebanonBenignBreast CancerJalkh et al, 2012 16 unrelated patients with breast cancer
© CAGS 2024. All rights reserved.