Apolipoprotein L1 (APOL1) Renal Risk Variant Genotyping
Also known as: APOL1: G1 and G2 allele, Apolipoprotein L1 Nephropathy, APOL1 Risk alleles, APO L1, APOL1 Genotyping
Use
This test detects genetic variants in the APOL1 gene—specifically the G1 (c.1024A>G & c.1152T>G) and G2 (c.1164_1169del) risk alleles—which increase susceptibility to certain forms of non-diabetic kidney disease. Individuals with two risk alleles (G1/G1, G1/G2, or G2/G2) are classified as having a “high‑risk genotype” and face a higher risk of progressive CKD, focal segmental glomerulosclerosis (FSGS), and end‑stage kidney disease compared with those with 0 or 1 risk allele (“low‑risk genotype”) ([questdiagnostics.com](https://www.questdiagnostics.com/healthcare-professionals/clinical-education-center/faq/faq287?utm_source=openai)).
Special Instructions
Not provided.
Limitations
Not provided.
Methodology
Sanger
Biomarkers
Result Turnaround Time
Not provided.
Related Documents
For more information, please review the documents below
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