rs9647379

This variant is located in the FNDC3B gene.

GWAS Catalog Trait Associations (5)

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

heart rate

Allele C
OR 0.02
p 3.0e-25
N 394,642
Large GWAS
European
Allele C
OR 0.21
p 1.0e-9
N 92,355
Large GWAS
multi-ancestry

appendicular lean mass

Allele C
OR 0.02
p 3.0e-21
N 450,243
Major Consortium StudyLarge GWAS
European
Hernandez Cordero AI et al. Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2. American Journal of Human Genetics 105(6):1222-1236 (2019)
Allele C
OR 0.04
p 2.0e-9
N 181,862
Large GWAS
European

hypertrophic cardiomyopathy

Allele C
OR 1.20
p 8.0e-11
N 8,361
Large GWAS
European
Allele C
OR 0.18
p 4.0e-10
N 42,802
Large GWAS
European, African unspecified, Hispanic or Latin American, East Asian, South Asian, NR

About FNDC3B

Enables RNA binding activity. Predicted to act upstream of or within several processes, including negative regulation of osteoblast differentiation; substrate adhesion-dependent cell spreading; and type II pneumocyte differentiation. Predicted to be located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]

View all FNDC3B variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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