rs55726687

This variant is located in the WNK1 gene.

GWAS Catalog Trait Associations (9)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

body mass index

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele G
OR 0.03
p 8.0e-12
N 607,406
Major Consortium StudyLarge GWAS
multi-ancestry
Allele G
OR 0.02
p 6.0e-20
N 394,642
Large GWAS
European
Harris BHL et al. New role of fat-free mass in cancer risk linked with genetic predisposition. Scientific Reports 14(1):7270 (2024)
Allele G
OR 0.02
p 8.0e-15
N 342,566
Large GWAS
European

base metabolic rate measurement

Allele A
OR 0.01
p 3.0e-21
N 394,642
Large GWAS
European

body weight

Allele A
OR 0.02
p 4.0e-21
N 394,642
Large GWAS
European
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.03
p 3.0e-12
N 609,198
Major Consortium StudyLarge GWAS
multi-ancestry

body height

Allele G
OR 0.01
p 3.0e-16
N 453,169
Large GWAS
European

hip circumference

Allele A
OR 0.02
p 2.0e-14
N 394,642
Large GWAS
European

fat pad mass

Harris BHL et al. New role of fat-free mass in cancer risk linked with genetic predisposition. Scientific Reports 14(1):7270 (2024)
Allele A
OR 0.02
p 4.0e-14
N 337,196
Large GWAS
European
Allele A
OR 0.02
p 1.0e-13
N 394,642
Large GWAS
European

visceral adipose tissue quantity

Allele A
OR 0.02
p 8.0e-14
N 325,153
Large GWAS
European

Abnormality of the skeletal system

Allele A
OR 0.01
p 6.0e-15
N 394,642
Large GWAS
European

ClinVar annotation

Benign★★★
2 submitters1 publication
View on ClinVar →

About WNK1

This gene encodes a member of the WNK subfamily of serine/threonine protein kinases. The encoded protein may be a key regulator of blood pressure by controlling the transport of sodium and chloride ions. Mutations in this gene have been associated with pseudohypoaldosteronism type II and hereditary sensory neuropathy type II. Alternatively spliced transcript variants encoding different isoforms have been described but the full-length nature of all of them has yet to be determined.[provided by RefSeq, May 2010]

View all WNK1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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