rs2279008

This is a upstream gene variant variant in the MYO9B gene.

GWAS Catalog Trait Associations (4)

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

body height

Allele C
OR 0.02
p 3.0e-20
N 455,180
Large GWAS
Hispanic or Latin American
Allele C
OR
β 0.025
p 3.0e-8
N 133,653
Large GWAS
European

sex hormone-binding globulin measurement

Sinnott-Armstrong N et al. Genetics of 35 blood and urine biomarkers in the UK Biobank. Nature Genetics 53(2):185-194 (2021)
Allele C
OR 0.02
p 6.0e-14
N 322,484
Major Consortium StudyLarge GWAS
multi-ancestry

health trait

Allele T
OR 0.01
p 1.0e-9
N 405,979
Large GWAS
European

HbA1c measurement

Sinnott-Armstrong N et al. Genetics of 35 blood and urine biomarkers in the UK Biobank. Nature Genetics 53(2):185-194 (2021)
Allele C
OR 0.02
p 2.0e-9
N 338,919
Major Consortium StudyLarge GWAS
multi-ancestry

About MYO9B

This gene encodes a member of the myosin family of actin-based molecular motor heavy chain proteins. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-9 (MYH9). The protein has four IQ motifs located in the neck domain that bind calmodulin, which serves as a light chain. The protein complex has a single-headed structure and exhibits processive movement on actin filaments toward the minus-end. The protein also has rho-GTPase activity. Polymorphisms in this gene are associated with celiac disease and ulcerative colitis susceptibility. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

View all MYO9B variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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