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GWAS Study

Rare variants in the DNA repair pathway and the risk of colorectal cancer.

Matejcic M, Shaban HA, Quintana MW et al.

33627384 PubMed ID
GWAS Study Type
5293 Participants
95 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MM
Matejcic M
SH
Shaban HA
QM
Quintana MW
SF
Schumacher FR
EC
Edlund CK
NL
Naghi L
PR
Pai RK
HR
Haile RW
LA
Levine AJ
BD
Buchanan DD
JM
Jenkins MA
FJ
Figueiredo JC
RG
Rennert G
GS
Gruber SB
LL
Li L
CG
Casey G
CD
Conti DV
SS
Schmit SL
Chapter II

Abstract

Summary of the research findings

Inherited susceptibility is an important contributor to colorectal cancer risk, and rare variants in key genes or pathways could account in part for the missing proportion of colorectal cancer heritability.

2,327 European ancestry cases, 2,966 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

5293
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Israel, U.S., Australia
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

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