AllergiesasthmaEvidence 3

rs75446656 · JMJD1C

Risk-Allele Phenotype

JMJD1C rs75446656 — associated with Asthma based on genetic association studies.

Reference-Allele Phenotype

Normal JMJD1C 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 — rs75446656
ClinVar — search rs75446656
NCBI Gene — JMJD1C

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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