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GWAS Study

Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height.

Hawkes G, Beaumont RN, Li Z et al.

39362880 PubMed ID
GWAS Study Type
304961 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HG
Hawkes G
BR
Beaumont RN
LZ
Li Z
MR
Mandla R
LX
Li X
AC
Albert CM
AD
Arnett DK
AA
Ashley-Koch AE
AA
Ashrani AA
BK
Barnes KC
BE
Boerwinkle E
BJ
Brody JA
CA
Carson AP
CN
Chami N
CY
Chen YI
CM
Chung MK
CJ
Curran JE
DD
Darbar D
EP
Ellinor PT
FM
Fornage M
GV
Gordeuk VR
GX
Guo X
HJ
He J
HC
Hwu CM
KR
Kalyani RR
KR
Kaplan R
KS
Kardia SLR
KC
Kooperberg C
LR
Loos RJF
LS
Lubitz SA
MR
Minster RL
NT
Naseri T
VS
Viali S
MB
Mitchell BD
MJ
Murabito JM
PN
Palmer ND
PB
Psaty BM
RS
Redline S
SM
Shoemaker MB
SE
Silverman EK
TM
Telen MJ
WS
Weiss ST
YL
Yanek LR
ZH
Zhou H
LC
Liu CT
NK
North KE
JA
Justice AE
LJ
Locke JM
ON
Owens N
MA
Murray A
PK
Patel K
FT
Frayling TM
WC
Wright CF
WA
Wood AR
LX
Lin X
MA
Manning A
WM
Weedon MN
Chapter II

Abstract

Summary of the research findings

The role of rare non-coding variation in complex human phenotypes is still largely unknown. To elucidate the impact of rare variants in regulatory elements, we performed a whole-genome sequencing association analysis for height using 333,100 individuals from three datasets: UK Biobank (N = 200,003), TOPMed (N = 87,652) and All of Us (N = 45,445). We performed rare ( < 0.1% minor-allele-frequency) single-variant and aggregate testing of non-coding variants in regulatory regions based on proximal-regulatory, intergenic-regulatory and deep-intronic annotation. We observed 29 independent variants associated with height at P < 6 × 10 - 10 after conditioning on previously reported variants, with effect sizes ranging from -7cm to +4.7 cm. We also identified and replicated non-coding aggregate-based associations proximal to HMGA1 containing variants associated with a 5 cm taller height and of highly-conserved variants in MIR497HG on chromosome 17. We have developed an approach for identifying non-coding rare variants in regulatory regions with large effects from whole-genome sequencing data associated with complex traits.

183,078 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

304961
Total Participants
GWAS
Study Type
Yes
Replicated
1,275 Samoan ancestry individuals, 3,845 East Asian ancestry individuals, 43,914 European individuals, 22,386 African American individuals, 1,236 Asian ancestry individuals, 14,996 Hispanic or Latin American individuals, 20,548 African ancestry individuals, 13,683 South Asian ancestry individuals
Replication Participants
European, Oceanian, East Asian, African American or Afro-Caribbean, Asian unspecified, Hispanic or Latin American, African unspecified, South Asian
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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