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GWAS Study

Genome-wide association study identifies multiple risk loci for renal cell carcinoma.

Scelo G, Purdue MP, Brown KM et al.

28598434 PubMed ID
GWAS Study Type
40673 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SG
Scelo G
PM
Purdue MP
BK
Brown KM
JM
Johansson M
WZ
Wang Z
EJ
Eckel-Passow JE
YY
Ye Y
HJ
Hofmann JN
CJ
Choi J
FM
Foll M
GV
Gaborieau V
MM
Machiela MJ
CL
Colli LM
LP
Li P
SJ
Sampson JN
AB
Abedi-Ardekani B
BC
Besse C
BH
Blanche H
BA
Boland A
BL
Burdette L
CA
Chabrier A
DG
Durand G
LC
Le Calvez-Kelm F
PE
Prokhortchouk E
RN
Robinot N
SK
Skryabin KG
WM
Wozniak MB
YM
Yeager M
BG
Basta-Jovanovic G
DZ
Dzamic Z
FL
Foretova L
HI
Holcatova I
JV
Janout V
MD
Mates D
MA
Mukeriya A
RS
Rascu S
ZD
Zaridze D
BV
Bencko V
CC
Cybulski C
FE
Fabianova E
JV
Jinga V
LJ
Lissowska J
LJ
Lubinski J
NM
Navratilova M
RP
Rudnai P
SN
Szeszenia-Dabrowska N
BS
Benhamou S
CG
Cancel-Tassin G
CO
Cussenot O
BL
Baglietto L
BH
Boeing H
KK
Khaw KT
WE
Weiderpass E
LB
Ljungberg B
SR
Sitaram RT
BF
Bruinsma F
JS
Jordan SJ
SG
Severi G
WI
Winship I
HK
Hveem K
VL
Vatten LJ
FT
Fletcher T
KK
Koppova K
LS
Larsson SC
WA
Wolk A
BR
Banks RE
SP
Selby PJ
ED
Easton DF
PP
Pharoah P
AG
Andreotti G
FL
Freeman LEB
KS
Koutros S
AD
Albanes D
MS
Männistö S
WS
Weinstein S
CP
Clark PE
ET
Edwards TL
LL
Lipworth L
GS
Gapstur SM
SV
Stevens VL
CH
Carol H
FM
Freedman ML
PM
Pomerantz MM
CE
Cho E
KP
Kraft P
PM
Preston MA
WK
Wilson KM
MG
Michael Gaziano J
SH
Sesso HD
BA
Black A
FN
Freedman ND
HW
Huang WY
AJ
Anema JG
KR
Kahnoski RJ
LB
Lane BR
NS
Noyes SL
PD
Petillo D
TB
Teh BT
PU
Peters U
WE
White E
AG
Anderson GL
JL
Johnson L
LJ
Luo J
BJ
Buring J
LI
Lee IM
CW
Chow WH
ML
Moore LE
WC
Wood C
ET
Eisen T
HM
Henrion M
LJ
Larkin J
BP
Barman P
LB
Leibovich BC
CT
Choueiri TK
ML
Mark Lathrop G
RN
Rothman N
DJ
Deleuze JF
MJ
McKay JD
PA
Parker AS
WX
Wu X
HR
Houlston RS
BP
Brennan P
CS
Chanock SJ
Chapter II

Abstract

Summary of the research findings

Previous genome-wide association studies (GWAS) have identified six risk loci for renal cell carcinoma (RCC). We conducted a meta-analysis of two new scans of 5,198 cases and 7,331 controls together with four existing scans, totalling 10,784 cases and 20,406 controls of European ancestry. Twenty-four loci were tested in an additional 3,182 cases and 6,301 controls. We confirm the six known RCC risk loci and identify seven new loci at 1p32.3 (rs4381241, P=3.1 × 10-10), 3p22.1 (rs67311347, P=2.5 × 10-8), 3q26.2 (rs10936602, P=8.8 × 10-9), 8p21.3 (rs2241261, P=5.8 × 10-9), 10q24.33-q25.1 (rs11813268, P=3.9 × 10-8), 11q22.3 (rs74911261, P=2.1 × 10-10) and 14q24.2 (rs4903064, P=2.2 × 10-24). Expression quantitative trait analyses suggest plausible candidate genes at these regions that may contribute to RCC susceptibility.

10,784 European ancestry cases, 20,406 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

40673
Total Participants
GWAS
Study Type
Yes
Replicated
3,182 European ancestry cases, 6,301 European ancestry controls
Replication Participants
European
Ancestry
U.S., Australia, Czech Republic, Poland, Romania, Russian Federation, Sweden, Serbia, France, Hungary, Slovakia, Finland, Norway, U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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