Variant (rsID / SNP)

rs136177

rs136177 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOL1. Location: chromosome 22, position 36,661,842. Clinical significance in the table: Benign.

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Reference-table entries

APOL1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:36661842
Cytoband: 22q12.3
HGVS: NM_003661.4(APOL1):c.960G>A (p.Arg320=)
Allele change: Synonymous_R320R

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.