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GWAS Study

Common and rare susceptibility genetic variants predisposing to Brugada Syndrome in Thailand.

Makarawate P, Glinge C, Khongphatthanayothin A et al.

32619740 PubMed ID
GWAS Study Type
586 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MP
Makarawate P
GC
Glinge C
KA
Khongphatthanayothin A
WR
Walsh R
MJ
Mauleekoonphairoj J
AM
Amnueypol M
PS
Prechawat S
WW
Wongcharoen W
KR
Krittayaphong R
AA
Anannab A
LP
Lichtner P
MT
Meitinger T
TF
Tjong FVY
LK
Lieve KVV
AA
Amin AS
SD
Sahasatas D
NT
Ngarmukos T
WD
Wichadakul D
PS
Payungporn S
SB
Sutjaporn B
WP
Wandee P
PY
Poovorawan Y
TJ
Tfelt-Hansen J
TM
Tanck MWT
TR
Tadros R
WA
Wilde AAM
BC
Bezzina CR
VG
Veerakul G
NK
Nademanee K
Chapter II

Abstract

Summary of the research findings

Mutations in SCN5A are rarely found in Thai patients with Brugada syndrome (BrS). Recent evidence suggested that common genetic variations may underlie BrS in a complex inheritance model.

154 Thai cases, 432 Thai controls

Chapter III

Study Statistics

Key metrics and study information

586
Total Participants
GWAS
Study Type
No
Replicated
South East Asian
Ancestry
Thailand
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.