Gene: CENPW
Alternate names for this Gene: C6orf173|CENP-W|CUG2
Gene Summary:
Gene is located in Chromosome: 6
Location in Chromosome : 6q22.32
Description of this Gene: centromere protein W
Type of Gene: protein-coding
rs1361108 in
CENPW gene and
Age at menarche
PMID 21102462 2010 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
PMID 25231870 2014 Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.
rs9388490 in
CENPW gene and
Alopecia
PMID 28196072 2017 Genetic prediction of male pattern baldness.
rs9398803 in
CENPW gene and
Alopecia, Androgenetic, 1
PMID 29146897 2017 GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
rs9398803 in
CENPW gene and
Alopecia, Androgenetic, 2
PMID 29146897 2017 GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
rs9398803 in
CENPW gene and
Alopecia, Androgenetic, 3
PMID 29146897 2017 GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
rs9398803 in
CENPW gene and
Alopecia, Male Pattern
PMID 29146897 2017 GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
rs9398803 in
CENPW gene and
Androgenetic Alopecia
PMID 29146897 2017 GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
rs1578060 in
CENPW gene and
Body Height
PMID 28270201 2017 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
rs1591805 in
CENPW gene and
Coronary Artery Disease
PMID 29212778 2018 Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
rs1538171 in
CENPW gene and
Diabetes Mellitus, Insulin-Dependent
PMID 25751624 2015 Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers.
PMID 19430480 2009 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.
rs11759026 in
CENPW gene and
Diabetes Mellitus, Non-Insulin-Dependent
PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
PMID 28869590 2017 Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease.
rs9385399 in
CENPW gene and
Infant length
PMID 25281659 2015 A novel common variant in DCST2 is associated with length in early life and height in adulthood.
rs9388487 in
CENPW gene and
Intelligence
PMID 29844566 2018 Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
PMID 29326435 2019 A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.
rs9388490 in
CENPW gene and
Lean body mass
PMID 30593698 2019 Genomics of body fat percentage may contribute to sex bias in anorexia nervosa.
rs9388489 in
CENPW gene and
Multiple Sclerosis
PMID 22190364 2011 Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
rs9398803 in
CENPW gene and
Other alopecia
PMID 29146897 2017 GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
rs1361108 in
CENPW gene and
Tonometry
PMID 29617998 2018 Genome-wide association analyses identify new loci influencing intraocular pressure.
rs11759026 in
CENPW gene and
Vital capacity
PMID 30061609 2018 Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.
PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
rs1591805 in
CENPW gene and
body fat percentage (physical finding)
PMID 30593698 2019 Genomics of body fat percentage may contribute to sex bias in anorexia nervosa.
rs9388490 in
CENPW gene and
mathematical ability
PMID 30038396 2018 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.