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GWAS Study

Common sequence variants on 20q11.22 confer melanoma susceptibility.

Brown KM, Macgregor S, Montgomery GW et al.

18488026 PubMed ID
GWAS Study Type
4209 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

BK
Brown KM
MS
Macgregor S
MG
Montgomery GW
CD
Craig DW
ZZ
Zhao ZZ
IK
Iyadurai K
HA
Henders AK
HN
Homer N
CM
Campbell MJ
SM
Stark M
TS
Thomas S
SH
Schmid H
HE
Holland EA
GE
Gillanders EM
DD
Duffy DL
MJ
Maskiell JA
JJ
Jetann J
FM
Ferguson M
SD
Stephan DA
CA
Cust AE
WD
Whiteman D
GA
Green A
OH
Olsson H
PS
Puig S
GP
Ghiorzo P
HJ
Hansson J
DF
Demenais F
GA
Goldstein AM
GN
Gruis NA
ED
Elder DE
BJ
Bishop JN
KR
Kefford RF
GG
Giles GG
AB
Armstrong BK
AJ
Aitken JF
HJ
Hopper JL
MN
Martin NG
TJ
Trent JM
MG
Mann GJ
HN
Hayward NK
Chapter II

Abstract

Summary of the research findings

We conducted a genome-wide association pooling study for cutaneous melanoma and performed validation in samples totaling 2,019 cases and 2,105 controls. Using pooling, we identified a new melanoma risk locus on chromosome 20 (rs910873 and rs1885120), with replication in two further samples (combined P < 1 x 10(-15)). The per allele odds ratio was 1.75 (1.53, 2.01), with evidence for stronger association in early-onset cases.

864 European ancestry cases, 864 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

4209
Total Participants
GWAS
Study Type
Yes
Replicated
1,230 European ancestry cases, 1,251 European ancestry controls
Replication Participants
European
Ancestry
Australia
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.