AllergiesbarrierEvidence 3

rs11242709 · LINC03066

Risk-Allele Phenotype

LINC03066 rs11242709 — associated with Eczema based on genetic association studies.

Reference-Allele Phenotype

Normal LINC03066 function at this locus, with no elevated genetic risk contribution to Eczema from this variant.

Evidence Level

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

Cross-References

dbSNP — rs11242709
ClinVar — search rs11242709
NCBI Gene — LINC03066

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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