Variant (rsID / SNP)
rs60910145
rs60910145 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOL1. Location: chromosome 22, position 36,662,034. Clinical significance in the table: Benign; risk factor.
Reference-table entries
APOL1Benign
- Clinical significance (as recorded)
- Benign; risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 22:36662034
- Cytoband
- 22q12.3
- HGVS
- NM_003661.4(APOL1):c.1152T>G (p.Ile384Met)
- Allele change
- Missense_I384M
Associated conditions / phenotypes
Hyalinosis, Segmental Glomerular|Glomerulonephritis|Proteinuria|Focal segmental glomerulosclerosis|Steroid-resistant nephrotic syndrome|Focal segmental glomerulosclerosis|Focal segmental glomerulosclerosis|Sickled erythrocytes|Nephrotic range proteinuria
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.