AllergiesasthmaEvidence 3

rs11716087 · LINC01208

Risk-Allele Phenotype

LINC01208 rs11716087 — associated with Atopic asthma based on genetic association studies.

Reference-Allele Phenotype

Normal LINC01208 function at this locus, with no elevated genetic risk contribution to Atopic asthma from this variant.

Evidence Level

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

Cross-References

dbSNP — rs11716087
ClinVar — search rs11716087
NCBI Gene — LINC01208

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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