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GWAS Study

Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas.

Hoffman J, Fejerman L, Hu D et al.

30642363 PubMed ID
GWAS Study Type
31182 Participants
71 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HJ
Hoffman J
FL
Fejerman L
HD
Hu D
HS
Huntsman S
LM
Li M
JE
John EM
TG
Torres-Mejia G
KL
Kushi L
DY
Ding YC
WJ
Weitzel J
NS
Neuhausen SL
LP
Lott P
EM
Echeverry M
CL
Carvajal-Carmona L
BE
Burchard E
EC
Eng C
LJ
Long J
ZW
Zheng W
OO
Olopade O
HD
Huo D
HC
Haiman C
ZE
Ziv E
Chapter II

Abstract

Summary of the research findings

Breast cancer is a partially heritable trait and genome-wide association studies (GWAS) have identified over 180 common genetic variants associated with breast cancer. We have previously performed breast cancer GWAS in Latinas and identified a strongly protective single nucleotide polymorphism (SNP) at 6q25, with the protective minor allele originating from indigenous American ancestry. Here we report on fine mapping of the 6q25 locus in an expanded sample of Latinas.

2,385 Latina cases, 6,416 Latina controls

Chapter III

Study Statistics

Key metrics and study information

31182
Total Participants
GWAS
Study Type
Yes
Replicated
2,412 Latina cases, 1,580 Latina controls, 3,153 African American cases, 2,831 African American controls, 1,657 African, African American and West Indian cases, 2,029 African, African American and West Indian controls, 4,525 East Asian ancestry cases, 4,194 East Asian ancestry controls, European ancestry cases, European ancestry controls
Replication Participants
European, Hispanic or Latin American, African American or Afro-Caribbean, East Asian, African unspecified, African American or Afro-Caribbean
Ancestry
Mexico, U.S., Colombia, China
Recruitment Country
Chapter IV

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