NM_001146274.1:c.552+7162G>C

  1. Home
  2. NM_001146274.1:c.552+7162G>C

HGVS Expressions

  • NG_012631.1:g.102039G>C
  • NM_001146274.1:c.552+7162G>C
  • NC_000010.11:g.113047288G>C

Associated Genes

Transcription Factor 7-Like 2
Back to search Result
Clinvar Clinical Significance

Risk factor

Variant Type

Substitution

dbSNP

11196205

Clinvar

7415

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.7.1Lebanon6490.47Type 2 Diabetes MellitusNemr et al, 2012c Study with 691 T2DM patients
125853.G.7.2Lebanon8560.47Nemr et al, 2012c Group consisting of 919 control subjects
Download Table

Contributors

  • Asha Deepthi: 25.05.2021

Edit History

  • Asha Deepthi: 25.05.2021
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.