NM_001080432.2:c.46-27777C>A

HGVS Expressions

  • NG_012969.1:g.83401C>A
  • NM_001080432.2:c.46-27777C>A
  • NP_001073901.1:p.?
  • NC_000016.10:g.53782363C>A
Back to search Result
CTGA Clinical Significance

Association, Benign

Variant Type

Substitution

dbSNP

8050136

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.32.3United Arab EmiratesNAAssociationType 2 Diabetes MellitusOsman et al. 2020 Study with 914 individuals. 36 SNPs show...
610966.G.2Lebanon2041BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
© CAGS 2024. All rights reserved.