NM_031885.5:c.940+36G>A

HGVS Expressions

  • NG_009312.2:g.22388G>A
  • NM_031885.5:c.940+36G>A
  • NC_000016.10:g.56502637C>T

Associated Genes

BBS2 Gene
Back to search Result
CTGA Clinical Significance

Benign

Variant Type

Substitution

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615982.6Saudi Arabia1BenignAbu-Safieh et al. 2012 "BBS-F031-A" in the publication
© CAGS 2024. All rights reserved.