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GWAS Study

A large Canadian cohort provides insights into the genetic architecture of human hair colour.

Lona-Durazo F, Mendes M, Thakur R et al.

34737440 PubMed ID
GWAS Study Type
12398 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LF
Lona-Durazo F
MM
Mendes M
TR
Thakur R
FK
Funderburk K
ZT
Zhang T
KM
Kovacs MA
CJ
Choi J
BK
Brown KM
PE
Parra EJ
Chapter II

Abstract

Summary of the research findings

Hair colour is a polygenic phenotype that results from differences in the amount and ratio of melanins located in the hair bulb. Genome-wide association studies (GWAS) have identified many loci involved in the pigmentation pathway affecting hair colour. However, most of the associated loci overlap non-protein coding regions and many of the molecular mechanisms underlying pigmentation variation are still not understood. Here, we conduct GWAS meta-analyses of hair colour in a Canadian cohort of 12,741 individuals of European ancestry. By performing fine-mapping analyses we identify candidate causal variants in pigmentation loci associated with blonde, red and brown hair colour. Additionally, we observe colocalization of several GWAS hits with expression and methylation quantitative trait loci (QTLs) of cultured melanocytes. Finally, transcriptome-wide association studies (TWAS) further nominate the expression of EDNRB and CDK10 as significantly associated with hair colour. Our results provide insights on the mechanisms regulating pigmentation biology in humans.

12,398 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

12398
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Canada
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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