NM_001146274.1:c.552+1640G>A

HGVS Expressions

  • NG_012631.1:g.96517G>A
  • NM_001146274.1:c.552+1640G>A
  • NC_000010.11:g.113041766G>A
Back to search Result
Variant Type

Substitution

dbSNP

7895340

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.7.1Lebanon6180.45Type 2 Diabetes MellitusNemr et al, 2012c Study with 691 T2DM patients
125853.G.7.2Lebanon7410.40Nemr et al, 2012c Group consisting of 919 control subjects
© CAGS 2024. All rights reserved.