AllergiesasthmaEvidence 3

rs2893907 · LINC02929

Risk-Allele Phenotype

LINC02929 rs2893907 — associated with Asthma based on genetic association studies.

Reference-Allele Phenotype

Normal LINC02929 function at this locus, with no elevated genetic risk contribution to Asthma from this variant.

Evidence Level

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

Cross-References

dbSNP — rs2893907
ClinVar — search rs2893907
NCBI Gene — LINC02929

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.

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