Variant (rsID / SNP)

rs2239785

rs2239785 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOL1. Location: chromosome 22, position 36,661,330. The table records no clinical significance for this variant.

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Reference-table entries

APOL1Not classified

Variant type: missense_variant
Chromosome / position: 22:36661330
HGVS: NM_145343.3,c.496G>A,p.Glu166Lys
Allele change: Missense_E150K

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.