NM_001318787.2:c.-372-616A>G

HGVS Expressions

  • NG_016229.1:g.8013A>G
  • NM_001318787.2:c.-372-616A>G

Associated Genes

Toll-Like Receptor 2
Back to search Result
Genomic Location

chr4:153687301

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

1898830

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
603028.G.1Lebanon2120.34AssociationHypertension, Essential; Hyperlipidemia, Familial Combined, 3Chedid et al. 2020 460 subjects (292 females, 168 males). G...
603028.G.2Lebanon1020.34AssociationHypertension, Essential; Hyperlipidemia, Familial Combined, 3Chedid et al. 2020 460 subjects (292 females, 168 males). G...
© CAGS 2024. All rights reserved.