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Variant (rsID / SNP)

rs136174

APOL1

rs136174 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOL1. Location: chromosome 22, position 36,661,536. The table records no clinical significance for this variant.

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Reference-table entries

APOL1Not classified
Variant type
synonymous_variant
Chromosome / position
22:36661536
HGVS
NM_145343.3,c.702C>A,p.Ala234Ala
Allele change
Synonymous_A218A

Public references

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