AllergiesasthmaEvidence 3

rs11144271 · OSTF1

Risk-Allele Phenotype

OSTF1 rs11144271 — associated with Asthma in muscoskeletal disease based on genetic association studies.

Reference-Allele Phenotype

Normal OSTF1 function at this locus, with no elevated genetic risk contribution to Asthma in muscoskeletal disease from this variant.

Evidence Level

3 — Limited — single study or in-vitro See methodology for how we grade evidence.

Cross-References

dbSNP — rs11144271
ClinVar — search rs11144271
NCBI Gene — OSTF1

Informational only

This page summarizes population-level evidence about a genetic variant. It is not a diagnosis. Your individual risk depends on your full genome, lifestyle, environment, and family history. Consult a healthcare provider for personalized medical advice.

Want to know your status at rs11144271?

Upload your DNA file — Atlagene checks this variant and 700+ others across 21 health categories.

Get Started Free