Variant (rsID / SNP)

rs11668789

rs11668789 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF584. Location: chromosome 19, position 58,928,309. The table records no clinical significance for this variant.

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Reference-table entries

ZNF584Not classified

Variant type: missense_variant
Chromosome / position: 19:58928309
HGVS: NM_173548.3,c.424C>T,p.Pro142Ser
Allele change: Missense_P97S

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.