PharmacogenomicsEvidence 3Physician review

rs5030868 · G6PD

Risk-Allele Phenotype

G6PD rs5030868 — classified as pathogenic; associated with G6PD MEDITERRANEAN. This variant has been identified as disease-causing with clinical evidence supporting its pathogenicity.

Reference-Allele Phenotype

Normal G6PD function at this locus, with no elevated genetic risk contribution to G6PD MEDITERRANEAN from this variant.

Evidence Level

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

Cross-References

dbSNP — rs5030868
ClinVar — search rs5030868
NCBI Gene — G6PD
PharmGKB — rs5030868

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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