Variant (rsID / SNP)

rs132736

rs132736 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOL4. Location: chromosome 22, position 36,598,058. The table records no clinical significance for this variant.

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Reference-table entries

APOL4Not classified

Variant type: missense_variant
Chromosome / position: 22:36598058
HGVS: NM_145660.2,c.25A>G,p.Ile9Val
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.