Variant (rsID / SNP)

rs3814538

rs3814538 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF462. Location: chromosome 9, position 109,691,676. The table records no clinical significance for this variant.

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Reference-table entries

ZNF462Not classified

Variant type: missense_variant
Chromosome / position: 9:109691676
HGVS: NM_021224.6,c.5483A>G,p.Asn1828Ser
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.