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GWAS Study

Genome-wide association study identifies common variants associated with breast cancer in South African Black women.

Hayat M, Chen WC, Babb de Villiers C et al.

40229280 PubMed ID
GWAS Study Type
3586 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HM
Hayat M
CW
Chen WC
BD
Babb de Villiers C
HL
Hyuck Lee S
CC
Curtis C
NR
Newton R
WT
Waterboer T
SF
Sitas F
BD
Bradshaw D
MM
Muchengeti M
SE
Singh E
LC
Lewis CM
RM
Ramsay M
MC
Mathew CG
BJ
Brandenburg JT
Chapter II

Abstract

Summary of the research findings

Genome-wide association studies (GWAS) have characterized the contribution of common variants to breast cancer (BC) risk in populations of European ancestry, however GWAS have not been reported in resident African populations. This GWAS included 2485 resident African BC cases and 1101 population matched controls. Two risk loci were identified, located between UNC13C and RAB27A on chromosome 15 (rs7181788, p = 1.01 × 10-08) and in USP22 on chromosome 17 (rs899342, p = 4.62 × 10-08). Several genome-wide significant signals were also detected in hormone receptor subtype analysis. The novel loci did not replicate in BC GWAS data from populations of West Africa ancestry suggesting genetic heterogeneity in different African populations, but further validation of these findings is needed. A European ancestry derived polygenic risk model for BC explained only 0.79% of variance in our data. Larger studies in pan-African populations are needed to further define the genetic contribution to BC risk.

2,485 Bantu-speaking African female cases, 1,101 Bantu-speaking African female controls

Chapter III

Study Statistics

Key metrics and study information

3586
Total Participants
GWAS
Study Type
No
Replicated
Sub-Saharan African
Ancestry
South Africa
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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