Variant (rsID / SNP)

rs136176

rs136176 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOL1. Location: chromosome 22, position 36,661,646. The table records no clinical significance for this variant.

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Reference-table entries

APOL1Not classified

Variant type: missense_variant
Chromosome / position: 22:36661646
HGVS: NM_145343.3,c.812G>A,p.Arg271Lys
Allele change: Missense_R255K

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.