Variant (rsID / SNP)

rs2032729

rs2032729 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF24. Location: chromosome 18, position 32,917,644. The table records no clinical significance for this variant.

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Reference-table entries

ZNF24Not classified

Variant type: missense_variant
Chromosome / position: 18:32917644
HGVS: NM_001375815.1,c.659A>G,p.Asn220Ser
Allele change: Missense_N220S

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.