Variant (rsID / SNP)

rs132653

rs132653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOL3. Location: chromosome 22, position 36,556,823. The table records no clinical significance for this variant.

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Reference-table entries

APOL3Not classified

Variant type: missense_variant
Chromosome / position: 22:36556823
HGVS: NM_145640.2,c.117C>A,p.Ser39Arg
Allele change: Silent

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.