Variant (rsID / SNP)

rs12986387

rs12986387 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF584. Location: chromosome 19, position 58,927,215. The table records no clinical significance for this variant.

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Reference-table entries

ZNF584Not classified

Variant type: missense_variant
Chromosome / position: 19:58927215
HGVS: NM_001318002.2,c.298C>T,p.Arg100Cys
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.