RS60910145 APOL1

Health Risk Chr 22:36265988
Upload your DNA to see your genotype for this variant.
What This Variant Does
"The derived allele of coding SNP rs60910145 (p.I384M) defines, together with the derived allele of c...
Associated Conditions
GWAS Studies (11)
Trait Risk Allele OR / Beta P-value Study
Chronic renal failure [CKD] (PheCode 585.3) T OR: 0.14 3E-26 PubMed
Chronic renal failure [CKD] (PheCode 585.3) T OR: 0.14 7E-26 PubMed
Disorders of calcium/phosphorus metabolism (PheCode 275.5) T OR: 0.3 4E-22 PubMed
Renal failure (PheCode 585) T OR: 0.11 6E-20 PubMed
Disorders of phosphorus metabolism (PheCode 275.53) T OR: 0.36 2E-19 PubMed
Renal failure (PheCode 585) T OR: 0.11 2E-19 PubMed
Hypertensive heart and/or renal disease (PheCode 401.2) T OR: 0.12 3E-18 PubMed
Hypertensive heart and/or renal disease (PheCode 401.2) T OR: 0.11 4E-18 PubMed
Kidney disease with dialysis T OR: 0.44 9E-16 PubMed
Kidney disease with dialysis T OR: 0.42 2E-14 PubMed
Takes medication for kidney disease with dialysis? T OR: 0.4 4E-13 PubMed
Other Variants in APOL1
Ask Dr. Hemsworth about this variant