AllergiesasthmaEvidence 3

rs74538397 · LINC01127

Risk-Allele Phenotype

LINC01127 rs74538397 — associated with Nonatopic asthma based on genetic association studies.

Reference-Allele Phenotype

Normal LINC01127 function at this locus, with no elevated genetic risk contribution to Nonatopic asthma from this variant.

Evidence Level

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

Cross-References

dbSNP — rs74538397
ClinVar — search rs74538397
NCBI Gene — LINC01127

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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