rs2609255

This is a intron variant variant in the FAM13A gene.

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GWAS Catalog Trait Associations (1)

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

interstitial lung disease

Fingerlin TE et al. “Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.” Nature Genetics 45(6):613-20 (2013)

Allele G

OR 1.29

p 2.0e-11

N 5,844

Large GWAS

European

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ClinVar annotation

Association

1 submitter

Chronic obstructive pulmonary disease; Combined pulmonary fibrosis-emphysema syndrome; Interstitial lung disease 2 (ILD2); Susceptibility to severe coronavirus disease (COVID-19)

View on ClinVar →

About FAM13A

Predicted to enable GTPase activator activity. Predicted to be involved in regulation of small GTPase mediated signal transduction. Predicted to be located in cytosol. Implicated in chronic obstructive pulmonary disease. [provided by Alliance of Genome Resources, Jul 2025]

View all FAM13A variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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